Primary Site >> Stomach Cancer
Gene >> TRPC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142806074:142806074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538677775 |
| CDS Mutation | c.2221C>T |
| AA Mutation | p.Arg741Cys(p.R741C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142736453:142736453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.247C>A |
| AA Mutation | p.Leu83Ile(p.L83I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142724657:142724657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.98C>T |
| AA Mutation | p.Ala33Val(p.A33V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142724567:142724567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8C>T |
| AA Mutation | p.Ala3Val(p.A3V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142806168:142806168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2315G>A |
| AA Mutation | p.Arg772Gln(p.R772Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142736429:142736429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223T>G |
| AA Mutation | p.Leu75Val(p.L75V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142736391:142736391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.185T>A |
| AA Mutation | p.Met62Lys(p.M62K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000476941 |
| Start | 142724731:142724731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.172G>A |
| AA Mutation | p.Gly58Ser(p.G58S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000476941 |
| Start | 142780995:142780995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748271979 |
| CDS Mutation | c.926G>A |
| AA Mutation | p.Arg309His(p.R309H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000476941 |
| Start | 142748377:142748377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.549A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000476941 |
| Start | 142780945:142780945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112064817 |
| CDS Mutation | c.876C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000476941 |
| Start | 142724595:142724595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758352959 |
| CDS Mutation | c.36G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000476941 |
| Start | 142748452:142748452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.624G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000476941 |
| Start | 142724628:142724629(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.69_70delAT |
| AA Mutation | p.Ser24LeufsTer24(p.S24Lfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000476941 |
| Start | 142748434:142748435(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.611dupA |
| AA Mutation | p.Asp205GlyfsTer2(p.D205Gfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |