Primary Site >> Stomach Cancer
Gene >> FLG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306584:152306584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8302G>C |
| AA Mutation | p.Glu2768Gln(p.E2768Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307288:152307288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754603159 |
| CDS Mutation | c.7598G>A |
| AA Mutation | p.Arg2533His(p.R2533H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313870:152313870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1016A>G |
| AA Mutation | p.His339Arg(p.H339R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307669:152307669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7217G>C |
| AA Mutation | p.Gly2406Ala(p.G2406A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310604:152310604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189279130 |
| CDS Mutation | c.4282C>T |
| AA Mutation | p.Arg1428Cys(p.R1428C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306583:152306583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8303A>C |
| AA Mutation | p.Glu2768Ala(p.E2768A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309391:152309391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772920605 |
| CDS Mutation | c.5495C>T |
| AA Mutation | p.Ser1832Leu(p.S1832L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310694:152310694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4192A>C |
| AA Mutation | p.Ser1398Arg(p.S1398R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312863:152312863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140188504 |
| CDS Mutation | c.2023G>T |
| AA Mutation | p.Asp675Tyr(p.D675Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307685:152307685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553468192 |
| CDS Mutation | c.7201C>T |
| AA Mutation | p.Arg2401Cys(p.R2401C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311396:152311396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3490A>C |
| AA Mutation | p.Thr1164Pro(p.T1164P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313939:152313939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376977047 |
| CDS Mutation | c.947C>T |
| AA Mutation | p.Ser316Leu(p.S316L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313530:152313530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1356G>C |
| AA Mutation | p.Glu452Asp(p.E452D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313057:152313057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200858156 |
| CDS Mutation | c.1829G>A |
| AA Mutation | p.Gly610Glu(p.G610E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303703:152303703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745539898 |
| CDS Mutation | c.11183G>T |
| AA Mutation | p.Gly3728Val(p.G3728V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307352:152307352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773788883 |
| CDS Mutation | c.7534A>C |
| AA Mutation | p.Ser2512Arg(p.S2512R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309493:152309493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141235242 |
| CDS Mutation | c.5393G>A |
| AA Mutation | p.Arg1798Gln(p.R1798Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307372:152307372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545692447 |
| CDS Mutation | c.7514A>G |
| AA Mutation | p.His2505Arg(p.H2505R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307291:152307291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7595C>T |
| AA Mutation | p.Ser2532Leu(p.S2532L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312607:152312607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2279A>G |
| AA Mutation | p.Gln760Arg(p.Q760R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313643:152313643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144799241 |
| CDS Mutation | c.1243C>T |
| AA Mutation | p.Arg415Trp(p.R415W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303142:152303142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11744C>A |
| AA Mutation | p.Ser3915Tyr(p.S3915Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304402:152304402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10484C>T |
| AA Mutation | p.Ser3495Leu(p.S3495L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308110:152308110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542918091 |
| CDS Mutation | c.6776G>A |
| AA Mutation | p.Arg2259Gln(p.R2259Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310057:152310057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148200894 |
| CDS Mutation | c.4829G>A |
| AA Mutation | p.Arg1610Gln(p.R1610Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303790:152303790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754536597 |
| CDS Mutation | c.11096G>A |
| AA Mutation | p.Arg3699Gln(p.R3699Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303166:152303166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554551056 |
| CDS Mutation | c.11720G>A |
| AA Mutation | p.Arg3907His(p.R3907H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312523:152312523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142483068 |
| CDS Mutation | c.2363G>A |
| AA Mutation | p.Arg788Gln(p.R788Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303449:152303449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11437A>G |
| AA Mutation | p.Thr3813Ala(p.T3813A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307129:152307129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7757C>T |
| AA Mutation | p.Ser2586Phe(p.S2586F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314278:152314278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.608G>T |
| AA Mutation | p.Arg203Ile(p.R203I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308732:152308732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6154G>C |
| AA Mutation | p.Glu2052Gln(p.E2052Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304886:152304886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776910156 |
| CDS Mutation | c.10000G>T |
| AA Mutation | p.Gly3334Trp(p.G3334W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305235:152305235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9651G>T |
| AA Mutation | p.Gln3217His(p.Q3217H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309446:152309446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772552807 |
| CDS Mutation | c.5440C>T |
| AA Mutation | p.Arg1814Cys(p.R1814C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312585:152312585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2301G>T |
| AA Mutation | p.Gln767His(p.Q767H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306542:152306542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748391293 |
| CDS Mutation | c.8344G>A |
| AA Mutation | p.Gly2782Ser(p.G2782S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307048:152307048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7838G>T |
| AA Mutation | p.Arg2613Ile(p.R2613I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313727:152313727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367578694 |
| CDS Mutation | c.1159G>A |
| AA Mutation | p.Gly387Ser(p.G387S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152302980:152302980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11906A>G |
| AA Mutation | p.Gln3969Arg(p.Q3969R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306883:152306883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8003C>T |
| AA Mutation | p.Ser2668Leu(p.S2668L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304972:152304972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147439082 |
| CDS Mutation | c.9914G>A |
| AA Mutation | p.Arg3305His(p.R3305H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314296:152314296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.590G>T |
| AA Mutation | p.Arg197Met(p.R197M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152302788:152302788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12098A>G |
| AA Mutation | p.Asn4033Ser(p.N4033S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309272:152309272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757686343 |
| CDS Mutation | c.5614A>G |
| AA Mutation | p.Lys1872Glu(p.K1872E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311179:152311179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201976711 |
| CDS Mutation | c.3707G>A |
| AA Mutation | p.Arg1236His(p.R1236H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313652:152313652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1234C>T |
| AA Mutation | p.Arg412Cys(p.R412C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314358:152314358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755044971 |
| CDS Mutation | c.528C>A |
| AA Mutation | p.Asn176Lys(p.N176K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307600:152307600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7286G>A |
| AA Mutation | p.Gly2429Glu(p.G2429E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308687:152308687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6199C>A |
| AA Mutation | p.Pro2067Thr(p.P2067T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314341:152314341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773896823 |
| CDS Mutation | c.545A>C |
| AA Mutation | p.Lys182Thr(p.K182T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313649:152313649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1237G>A |
| AA Mutation | p.Gly413Arg(p.G413R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305435:152305435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9451G>T |
| AA Mutation | p.Ala3151Ser(p.A3151S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313565:152313565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779690124 |
| CDS Mutation | c.1321G>A |
| AA Mutation | p.Gly441Arg(p.G441R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310247:152310247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4639G>A |
| AA Mutation | p.Glu1547Lys(p.E1547K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305057:152305057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9829C>T |
| AA Mutation | p.Arg3277Cys(p.R3277C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310723:152310723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368725307 |
| CDS Mutation | c.4163G>A |
| AA Mutation | p.Arg1388Gln(p.R1388Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313786:152313786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768202093 |
| CDS Mutation | c.1100G>C |
| AA Mutation | p.Gly367Ala(p.G367A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306581:152306581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8305C>A |
| AA Mutation | p.Gln2769Lys(p.Q2769K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306368:152306368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8518A>T |
| AA Mutation | p.Thr2840Ser(p.T2840S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309371:152309371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749467652 |
| CDS Mutation | c.5515T>C |
| AA Mutation | p.Ser1839Pro(p.S1839P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313536:152313536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1350C>A |
| AA Mutation | p.His450Gln(p.H450Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313190:152313190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1696A>C |
| AA Mutation | p.Ser566Arg(p.S566R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313670:152313670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200489906 |
| CDS Mutation | c.1216T>A |
| AA Mutation | p.Ser406Thr(p.S406T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308447:152308447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746864718 |
| CDS Mutation | c.6439G>C |
| AA Mutation | p.Gly2147Arg(p.G2147R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307334:152307334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111618175 |
| CDS Mutation | c.7552C>T |
| AA Mutation | p.Arg2518Cys(p.R2518C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303824:152303824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11062C>T |
| AA Mutation | p.His3688Tyr(p.H3688Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311083:152311083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3803C>A |
| AA Mutation | p.Ser1268Tyr(p.S1268Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306946:152306946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7940G>T |
| AA Mutation | p.Arg2647Ile(p.R2647I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313866:152313866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140261784 |
| CDS Mutation | c.1020T>G |
| AA Mutation | p.Asp340Glu(p.D340E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305083:152305083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9803C>A |
| AA Mutation | p.Ala3268Glu(p.A3268E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307352:152307352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7534A>G |
| AA Mutation | p.Ser2512Gly(p.S2512G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310765:152310765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4121G>T |
| AA Mutation | p.Gly1374Val(p.G1374V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310271:152310271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4615A>G |
| AA Mutation | p.Ser1539Gly(p.S1539G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303054:152303054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11832A>G |
| AA Mutation | p.Ile3944Met(p.I3944M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304348:152304348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143278829 |
| CDS Mutation | c.10538C>T |
| AA Mutation | p.Ala3513Val(p.A3513V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311483:152311483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372726892 |
| CDS Mutation | c.3403A>G |
| AA Mutation | p.Arg1135Gly(p.R1135G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303304:152303304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762274526 |
| CDS Mutation | c.11582C>T |
| AA Mutation | p.Ser3861Phe(p.S3861F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311224:152311224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202164130 |
| CDS Mutation | c.3662G>A |
| AA Mutation | p.Arg1221His(p.R1221H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305050:152305050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9836C>G |
| AA Mutation | p.Ala3279Gly(p.A3279G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305218:152305218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9668G>T |
| AA Mutation | p.Gly3223Val(p.G3223V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305051:152305051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115482787 |
| CDS Mutation | c.9835G>A |
| AA Mutation | p.Ala3279Thr(p.A3279T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307496:152307496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7390G>A |
| AA Mutation | p.Gly2464Arg(p.G2464R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313178:152313178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192402912 |
| CDS Mutation | c.1708C>A |
| AA Mutation | p.Gln570Lys(p.Q570K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306574:152306574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745721128 |
| CDS Mutation | c.8312A>G |
| AA Mutation | p.Gln2771Arg(p.Q2771R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313277:152313277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1609A>C |
| AA Mutation | p.Asn537His(p.N537H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313553:152313553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1333C>G |
| AA Mutation | p.Leu445Val(p.L445V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312215:152312215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2671A>C |
| AA Mutation | p.Ser891Arg(p.S891R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309130:152309130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5756G>T |
| AA Mutation | p.Ser1919Ile(p.S1919I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309605:152309605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149721675 |
| CDS Mutation | c.5281C>T |
| AA Mutation | p.Arg1761Cys(p.R1761C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313855:152313855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1031C>T |
| AA Mutation | p.Ala344Val(p.A344V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312434:152312434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147738817 |
| CDS Mutation | c.2452C>G |
| AA Mutation | p.Gln818Glu(p.Q818E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313589:152313589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1297G>T |
| AA Mutation | p.Asp433Tyr(p.D433Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312659:152312659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2227A>G |
| AA Mutation | p.Ser743Gly(p.S743G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312772:152312772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2114G>A |
| AA Mutation | p.Gly705Glu(p.G705E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308324:152308324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759067455 |
| CDS Mutation | c.6562A>C |
| AA Mutation | p.Ser2188Arg(p.S2188R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306317:152306317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762486668 |
| CDS Mutation | c.8569C>T |
| AA Mutation | p.Arg2857Cys(p.R2857C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310979:152310979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3907A>G |
| AA Mutation | p.Arg1303Gly(p.R1303G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307607:152307607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150216268 |
| CDS Mutation | c.7279G>A |
| AA Mutation | p.Ala2427Thr(p.A2427T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 100 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314507:152314507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.379A>G |
| AA Mutation | p.Ser127Gly(p.S127G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 101 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309860:152309860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5026A>G |
| AA Mutation | p.Ser1676Gly(p.S1676G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 102 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306352:152306352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8534A>G |
| AA Mutation | p.Glu2845Gly(p.E2845G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 103 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306306:152306306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8580A>C |
| AA Mutation | p.Glu2860Asp(p.E2860D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 104 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311243:152311243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3643A>C |
| AA Mutation | p.Ser1215Arg(p.S1215R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 105 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312186:152312186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2700A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 106 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308235:152308235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370184374 |
| CDS Mutation | c.6651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 107 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309954:152309954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763599249 |
| CDS Mutation | c.4932G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 108 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309555:152309555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145158439 |
| CDS Mutation | c.5331C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 109 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304926:152304926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201488619 |
| CDS Mutation | c.9960T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 110 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303840:152303840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573860455 |
| CDS Mutation | c.11046C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 111 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309192:152309192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545655284 |
| CDS Mutation | c.5694G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 112 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304821:152304821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10065G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 113 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310608:152310608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375923587 |
| CDS Mutation | c.4278C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 114 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303879:152303879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11007A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 115 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307767:152307767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7119A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 116 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313278:152313278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1608A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 117 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313656:152313656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766436341 |
| CDS Mutation | c.1230C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 118 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307377:152307377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7509C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 119 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314091:152314091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.795C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 120 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309750:152309750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5136A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 121 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313290:152313290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765626862 |
| CDS Mutation | c.1596C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 122 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312552:152312552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771168723 |
| CDS Mutation | c.2334C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 123 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312285:152312285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2601A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 124 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310680:152310680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4206A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 125 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308415:152308415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141369067 |
| CDS Mutation | c.6471G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 126 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310641:152310641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150981235 |
| CDS Mutation | c.4245A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 127 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310383:152310383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370219834 |
| CDS Mutation | c.4503G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 128 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310253:152310253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4633A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 129 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310359:152310359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4527A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 130 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304341:152304341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10545C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 131 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314391:152314391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.495A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 132 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310521:152310521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142950612 |
| CDS Mutation | c.4365C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 133 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304884:152304884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775583931 |
| CDS Mutation | c.10002G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 134 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311667:152311667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771660324 |
| CDS Mutation | c.3219T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 135 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310182:152310182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766533034 |
| CDS Mutation | c.4704C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 136 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310761:152310761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747250368 |
| CDS Mutation | c.4125C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 137 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314589:152314589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.297C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 138 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308913:152308913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138652718 |
| CDS Mutation | c.5973G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 139 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311403:152311403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3483T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 140 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311184:152311184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3702G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 141 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314409:152314409(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs746683647 |
| CDS Mutation | c.477delA |
| AA Mutation | p.Glu160LysfsTer34(p.E160Kfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 142 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368799 |
| Start | 152315394:152315394(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.63delA |
| AA Mutation | p.Asp22IlefsTer7(p.D22Ifs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 143 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306040:152306043(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.8843_8846delGACA |
| AA Mutation | p.Arg2948AsnfsTer118(p.R2948Nfs*118) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 144 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152307483:152307483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7403C>G |
| AA Mutation | p.Ser2468Ter(p.S2468*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 145 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152304999:152304999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761212672 |
| CDS Mutation | c.9887C>A |
| AA Mutation | p.Ser3296Ter(p.S3296*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 146 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152304946:152304946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9940A>T |
| AA Mutation | p.Arg3314Ter(p.R3314*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 147 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152311694:152311694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755119896 |
| CDS Mutation | c.3192G>A |
| AA Mutation | p.Trp1064Ter(p.W1064*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 148 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314336:152314337(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.549dupA |
| AA Mutation | p.Glu184ArgfsTer6(p.E184Rfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 149 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307564:152307565(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.7321dupT |
| AA Mutation | p.Ser2441PhefsTer44(p.S2441Ffs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 150 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306768:152306769(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.8117_8118insCACGA |
| AA Mutation | p.Val2707ThrfsTer38(p.V2707Tfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |