Primary Site >> Stomach Cancer
Gene >> SLC26A4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107674235:107674235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200229408 |
| CDS Mutation | c.487G>A |
| AA Mutation | p.Val163Ile(p.V163I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107694464:107694464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1325T>C |
| AA Mutation | p.Leu442Pro(p.L442P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107690165:107690165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1191C>G |
| AA Mutation | p.Phe397Leu(p.F397L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107700137:107700137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1669G>T |
| AA Mutation | p.Gly557Cys(p.G557C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107694473:107694473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1334T>C |
| AA Mutation | p.Leu445Ser(p.L445S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107710084:107710084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2120G>A |
| AA Mutation | p.Gly707Glu(p.G707E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107683287:107683287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Ala284Val(p.A284V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265715 |
| Start | 107694439:107694439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757552791 |
| CDS Mutation | c.1300G>A |
| AA Mutation | p.Ala434Thr(p.A434T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265715 |
| Start | 107701145:107701145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771015634 |
| CDS Mutation | c.1752G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265715 |
| Start | 107674222:107674222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.474C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265715 |
| Start | 107694672:107694672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265715 |
| Start | 107689119:107689119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1068C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265715 |
| Start | 107683207:107683207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.771G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265715 |
| Start | 107663392:107663392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758057358 |
| CDS Mutation | c.261C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265715 |
| Start | 107663338:107663338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.207G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265715 |
| Start | 107700155:107700155(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1692delA |
| AA Mutation | p.Lys564AsnfsTer19(p.K564Nfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265715 |
| Start | 107683495:107683495(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs747834704 |
| CDS Mutation | c.965delA |
| AA Mutation | p.Asn322IlefsTer22(p.N322Ifs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265715 |
| Start | 107675032:107675033(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.690dupA |
| AA Mutation | p.Val231SerfsTer29(p.V231Sfs*29) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |