Primary Site >> Stomach Cancer
Gene >> KALRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124482872:124482872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4250G>T |
| AA Mutation | p.Arg1417Met(p.R1417M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124334413:124334413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35057827 |
| CDS Mutation | c.1559G>A |
| AA Mutation | p.Arg520Gln(p.R520Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124518419:124518419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4949G>A |
| AA Mutation | p.Arg1650Gln(p.R1650Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124658443:124658443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.955C>T |
| AA Mutation | p.His319Tyr(p.H319Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124455285:124455285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3655C>G |
| AA Mutation | p.His1219Asp(p.H1219D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124384984:124384984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1904A>C |
| AA Mutation | p.Gln635Pro(p.Q635P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124650874:124650874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637G>A |
| AA Mutation | p.Ala213Thr(p.A213T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124632633:124632633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201792111 |
| CDS Mutation | c.299G>A |
| AA Mutation | p.Arg100Gln(p.R100Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124717345:124717345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3284A>G |
| AA Mutation | p.Gln1095Arg(p.Q1095R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124717270:124717270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3209A>T |
| AA Mutation | p.Asp1070Val(p.D1070V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360013 |
| Start | 124562928:124562928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375684753 |
| CDS Mutation | c.5015C>T |
| AA Mutation | p.Thr1672Met(p.T1672M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124268893:124268893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.601C>T |
| AA Mutation | p.Leu201Phe(p.L201F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124269243:124269243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768503730 |
| CDS Mutation | c.951G>T |
| AA Mutation | p.Gln317His(p.Q317H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124455274:124455274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148828057 |
| CDS Mutation | c.3644C>T |
| AA Mutation | p.Thr1215Met(p.T1215M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124702075:124702075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2943A>C |
| AA Mutation | p.Glu981Asp(p.E981D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124461914:124461914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3873G>C |
| AA Mutation | p.Gln1291His(p.Q1291H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124477318:124477318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759826348 |
| CDS Mutation | c.4169C>T |
| AA Mutation | p.Ala1390Val(p.A1390V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360013 |
| Start | 124562979:124562979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5066G>A |
| AA Mutation | p.Arg1689His(p.R1689H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124655646:124655646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.747G>T |
| AA Mutation | p.Lys249Asn(p.K249N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124413489:124413489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2360C>T |
| AA Mutation | p.Ala787Val(p.A787V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124496340:124496340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4856G>T |
| AA Mutation | p.Gly1619Val(p.G1619V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124446224:124446224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3371G>A |
| AA Mutation | p.Arg1124Gln(p.R1124Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124413567:124413567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367667422 |
| CDS Mutation | c.2438G>A |
| AA Mutation | p.Arg813His(p.R813H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124441985:124441985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3233A>C |
| AA Mutation | p.Lys1078Thr(p.K1078T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124384986:124384986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1906C>T |
| AA Mutation | p.Arg636Trp(p.R636W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291478 |
| Start | 124674367:124674367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775753465 |
| CDS Mutation | c.1855G>A |
| AA Mutation | p.Asp619Asn(p.D619N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124227999:124227999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754069791 |
| CDS Mutation | c.77G>A |
| AA Mutation | p.Arg26Gln(p.R26Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124455250:124455250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139468141 |
| CDS Mutation | c.3620C>T |
| AA Mutation | p.Thr1207Met(p.T1207M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124298817:124298817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.990G>T |
| AA Mutation | p.Lys330Asn(p.K330N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124482820:124482820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775145320 |
| CDS Mutation | c.4198C>T |
| AA Mutation | p.Arg1400Trp(p.R1400W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124384861:124384861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1781C>T |
| AA Mutation | p.Ala594Val(p.A594V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124413488:124413488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755363438 |
| CDS Mutation | c.2359G>A |
| AA Mutation | p.Ala787Thr(p.A787T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360013 |
| Start | 124563056:124563056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201338676 |
| CDS Mutation | c.5143G>A |
| AA Mutation | p.Val1715Met(p.V1715M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124384972:124384972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748480747 |
| CDS Mutation | c.1892G>A |
| AA Mutation | p.Arg631His(p.R631H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124430709:124430709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2757T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124442043:124442043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184463395 |
| CDS Mutation | c.3291C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291478 |
| Start | 124632442:124632442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367903538 |
| CDS Mutation | c.108C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124413544:124413544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775380051 |
| CDS Mutation | c.2415C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291478 |
| Start | 124666544:124666544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768846133 |
| CDS Mutation | c.1347C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124268976:124268976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.684C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124446780:124446780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3441A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124268883:124268883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368081230 |
| CDS Mutation | c.591C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291478 |
| Start | 124657761:124657761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.900T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124490767:124490767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375318950 |
| CDS Mutation | c.4464G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240874 |
| Start | 124455229:124455229(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs771832826 |
| CDS Mutation | c.3603delA |
| AA Mutation | p.Gly1202AlafsTer8(p.G1202Afs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |