Primary Site >> Stomach Cancer
Gene >> KRT6A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52491632:52491632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.645G>T |
| AA Mutation | p.Glu215Asp(p.E215D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52493145:52493145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533157590 |
| CDS Mutation | c.44G>A |
| AA Mutation | p.Arg15His(p.R15H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52490619:52490619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1027G>A |
| AA Mutation | p.Glu343Lys(p.E343K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52491138:52491138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790G>A |
| AA Mutation | p.Glu264Lys(p.E264K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52490943:52490943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747979011 |
| CDS Mutation | c.827C>T |
| AA Mutation | p.Ala276Val(p.A276V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52490877:52490877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.893T>C |
| AA Mutation | p.Leu298Pro(p.L298P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52487755:52487755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1660A>T |
| AA Mutation | p.Thr554Ser(p.T554S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52487842:52487842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1573G>T |
| AA Mutation | p.Gly525Cys(p.G525C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52491666:52491666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.611A>C |
| AA Mutation | p.Lys204Thr(p.K204T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52492900:52492900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200254647 |
| CDS Mutation | c.289G>A |
| AA Mutation | p.Gly97Arg(p.G97R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330722 |
| Start | 52490023:52490023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368272363 |
| CDS Mutation | c.1123C>T |
| AA Mutation | p.Arg375Cys(p.R375C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330722 |
| Start | 52492655:52492655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773542280 |
| CDS Mutation | c.534C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330722 |
| Start | 52492817:52492817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.372C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330722 |
| Start | 52490030:52490030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372043088 |
| CDS Mutation | c.1116C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330722 |
| Start | 52491539:52491539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330722 |
| Start | 52488088:52488088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756329465 |
| CDS Mutation | c.1440C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330722 |
| Start | 52488375:52488375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368523101 |
| CDS Mutation | c.1377C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330722 |
| Start | 52487906:52487906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376504088 |
| CDS Mutation | c.1509C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000330722 |
| Start | 52492793:52492794(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.395dupC |
| AA Mutation | p.Gly133TrpfsTer30(p.G133Wfs*30) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |