Primary Site >> Stomach Cancer
Gene >> CROCC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16930316:16930316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372750456 |
| CDS Mutation | c.652G>A |
| AA Mutation | p.Ala218Thr(p.A218T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16946344:16946344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2222T>G |
| AA Mutation | p.Leu741Arg(p.L741R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16924361:16924361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142411267 |
| CDS Mutation | c.233C>T |
| AA Mutation | p.Ser78Leu(p.S78L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16938937:16938937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1403T>C |
| AA Mutation | p.Val468Ala(p.V468A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16954264:16954264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3228G>T |
| AA Mutation | p.Glu1076Asp(p.E1076D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375541 |
| Start | 16938909:16938909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1375G>A |
| AA Mutation | p.Ala459Thr(p.A459T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16966056:16966056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4633G>A |
| AA Mutation | p.Glu1545Lys(p.E1545K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16970742:16970742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5759C>T |
| AA Mutation | p.Ala1920Val(p.A1920V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16924403:16924403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146983726 |
| CDS Mutation | c.275G>A |
| AA Mutation | p.Arg92His(p.R92H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375541 |
| Start | 16924438:16924438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200540396 |
| CDS Mutation | c.310C>T |
| AA Mutation | p.Arg104Cys(p.R104C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375541 |
| Start | 16938910:16938910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1376C>T |
| AA Mutation | p.Ala459Val(p.A459V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16938932:16938932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145341541 |
| CDS Mutation | c.1398C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16972428:16972428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6036C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16946399:16946399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770820304 |
| CDS Mutation | c.2277C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16969157:16969157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5118C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16940001:16940001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1716C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16940052:16940052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369379898 |
| CDS Mutation | c.1767C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16924434:16924434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769667982 |
| CDS Mutation | c.306C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375541 |
| Start | 16924440:16924440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774563422 |
| CDS Mutation | c.312C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |