Primary Site >> Stomach Cancer
Gene >> PARP10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143985254:143985254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.748C>G |
| AA Mutation | p.Leu250Val(p.L250V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143983673:143983673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1916C>A |
| AA Mutation | p.Pro639His(p.P639H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143983242:143983242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781999070 |
| CDS Mutation | c.2347C>T |
| AA Mutation | p.Arg783Cys(p.R783C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143983062:143983062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141244035 |
| CDS Mutation | c.2426C>T |
| AA Mutation | p.Ala809Val(p.A809V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143984953:143984953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1049G>C |
| AA Mutation | p.Ser350Thr(p.S350T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143984723:143984723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1279G>A |
| AA Mutation | p.Ala427Thr(p.A427T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143984428:143984428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1462T>C |
| AA Mutation | p.Cys488Arg(p.C488R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143983296:143983296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529405414 |
| CDS Mutation | c.2293C>T |
| AA Mutation | p.Arg765Cys(p.R765C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143983536:143983536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2053C>A |
| AA Mutation | p.Leu685Ile(p.L685I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143986130:143986130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782082984 |
| CDS Mutation | c.106C>T |
| AA Mutation | p.Arg36Cys(p.R36C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143985813:143985813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.344C>T |
| AA Mutation | p.Ala115Val(p.A115V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143977689:143977689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201667332 |
| CDS Mutation | c.2873G>A |
| AA Mutation | p.Arg958His(p.R958H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143983689:143983689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1900C>T |
| AA Mutation | p.His634Tyr(p.H634Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313028 |
| Start | 143984329:143984329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1561G>A |
| AA Mutation | p.Ala521Thr(p.A521T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313028 |
| Start | 143977814:143977814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782534075 |
| CDS Mutation | c.2748G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313028 |
| Start | 143985788:143985788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313028 |
| Start | 143985045:143985045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.957T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313028 |
| Start | 143984330:143984330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371073478 |
| CDS Mutation | c.1560C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313028 |
| Start | 143983007:143983007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574232624 |
| CDS Mutation | c.2481C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |