Primary Site >> Stomach Cancer
Gene >> TGFB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366930 |
| Start | 218434089:218434089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.518A>C |
| AA Mutation | p.Lys173Thr(p.K173T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366930 |
| Start | 218434194:218434194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.623A>G |
| AA Mutation | p.His208Arg(p.H208R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366930 |
| Start | 218434112:218434112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.541A>G |
| AA Mutation | p.Thr181Ala(p.T181A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366930 |
| Start | 218441258:218441258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376159002 |
| CDS Mutation | c.1141G>A |
| AA Mutation | p.Val381Met(p.V381M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366930 |
| Start | 218405279:218405279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.457C>T |
| AA Mutation | p.Arg153Cys(p.R153C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366930 |
| Start | 218434420:218434420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.726A>C |
| AA Mutation | p.Lys242Asn(p.K242N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366930 |
| Start | 218346875:218346875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775518697 |
| CDS Mutation | c.174T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366930 |
| Start | 218441257:218441257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201129153 |
| CDS Mutation | c.1140C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366930 |
| Start | 218346896:218346896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.195G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366930 |
| Start | 218434159:218434159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192335285 |
| CDS Mutation | c.588C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |