Primary Site >> Stomach Cancer
Gene >> ARHGEF40
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21084829:21084829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768330300 |
| CDS Mutation | c.3866G>A |
| AA Mutation | p.Arg1289His(p.R1289H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21074766:21074766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566211084 |
| CDS Mutation | c.1036G>A |
| AA Mutation | p.Gly346Arg(p.G346R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21074208:21074208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.478G>A |
| AA Mutation | p.Gly160Ser(p.G160S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21081687:21081687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2819G>A |
| AA Mutation | p.Arg940His(p.R940H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21081656:21081656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2788G>A |
| AA Mutation | p.Gly930Ser(p.G930S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21073234:21073234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763446664 |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Glu65Lys(p.E65K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21075117:21075117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1387G>T |
| AA Mutation | p.Gly463Trp(p.G463W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21074215:21074215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.485T>G |
| AA Mutation | p.Leu162Arg(p.L162R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21088843:21088843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4532C>T |
| AA Mutation | p.Ala1511Val(p.A1511V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21081635:21081635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2767C>T |
| AA Mutation | p.Arg923Trp(p.R923W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000298694 |
| Start | 21075497:21075497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143657914 |
| CDS Mutation | c.1616C>T |
| AA Mutation | p.Thr539Met(p.T539M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21074199:21074199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.469C>T |
| AA Mutation | p.Arg157Trp(p.R157W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21081002:21081002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370713697 |
| CDS Mutation | c.2626C>T |
| AA Mutation | p.Arg876Cys(p.R876C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298694 |
| Start | 21073972:21073972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749743127 |
| CDS Mutation | c.242C>T |
| AA Mutation | p.Pro81Leu(p.P81L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298694 |
| Start | 21075137:21075137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769226680 |
| CDS Mutation | c.1407C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298694 |
| Start | 21075168:21075168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298694 |
| Start | 21078926:21078926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2289C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298694 |
| Start | 21073973:21073973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114625560 |
| CDS Mutation | c.243G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298694 |
| Start | 21075014:21075014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298694 |
| Start | 21078445:21078445(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs749402223 |
| CDS Mutation | c.2209delG |
| AA Mutation | p.Ala737ProfsTer3(p.A737Pfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |