Primary Site >> Stomach Cancer
Gene >> DLGAP4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36431799:36431799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374922768 |
| CDS Mutation | c.82G>A |
| AA Mutation | p.Asp28Asn(p.D28N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36432246:36432246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765878319 |
| CDS Mutation | c.529G>A |
| AA Mutation | p.Gly177Ser(p.G177S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36431757:36431757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575670266 |
| CDS Mutation | c.40G>A |
| AA Mutation | p.Asp14Asn(p.D14N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36436244:36436244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1135G>A |
| AA Mutation | p.Asp379Asn(p.D379N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36432337:36432337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.620C>T |
| AA Mutation | p.Ser207Phe(p.S207F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36446803:36446803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1514A>T |
| AA Mutation | p.Tyr505Phe(p.Y505F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36436247:36436247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753922102 |
| CDS Mutation | c.1138G>A |
| AA Mutation | p.Glu380Lys(p.E380K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36436170:36436170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1061C>T |
| AA Mutation | p.Ala354Val(p.A354V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36496923:36496923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752019701 |
| CDS Mutation | c.1867C>T |
| AA Mutation | p.Arg623Trp(p.R623W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36432531:36432531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529565051 |
| CDS Mutation | c.814G>A |
| AA Mutation | p.Ala272Thr(p.A272T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36526879:36526879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114982034 |
| CDS Mutation | c.2827G>A |
| AA Mutation | p.Asp943Asn(p.D943N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36432247:36432247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530G>A |
| AA Mutation | p.Gly177Asp(p.G177D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36500341:36500341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376006423 |
| CDS Mutation | c.2242G>A |
| AA Mutation | p.Gly748Ser(p.G748S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36436317:36436317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1208A>T |
| AA Mutation | p.Gln403Leu(p.Q403L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36431803:36431803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367982678 |
| CDS Mutation | c.86G>A |
| AA Mutation | p.Arg29His(p.R29H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36500249:36500249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2150A>G |
| AA Mutation | p.Asp717Gly(p.D717G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36497031:36497031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1975G>T |
| AA Mutation | p.Ala659Ser(p.A659S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36432435:36432435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.718C>T |
| AA Mutation | p.Arg240Cys(p.R240C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36496758:36496758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1702A>G |
| AA Mutation | p.Thr568Ala(p.T568A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339266 |
| Start | 36432099:36432099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758516742 |
| CDS Mutation | c.382G>A |
| AA Mutation | p.Glu128Lys(p.E128K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339266 |
| Start | 36432176:36432176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.459G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339266 |
| Start | 36499635:36499635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2058C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339266 |
| Start | 36496991:36496991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1935A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339266 |
| Start | 36431738:36431738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.21C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339266 |
| Start | 36496724:36496724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373299123 |
| CDS Mutation | c.1668G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339266 |
| Start | 36497000:36497000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746042271 |
| CDS Mutation | c.1944G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339266 |
| Start | 36431837:36431837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528736011 |
| CDS Mutation | c.120C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000339266 |
| Start | 36442728:36442728(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1362delT |
| AA Mutation | p.Phe454LeufsTer6(p.F454Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |