Primary Site >> Stomach Cancer
Gene >> URGCP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878145:43878145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1318C>T |
| AA Mutation | p.Arg440Trp(p.R440W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43877449:43877449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201208471 |
| CDS Mutation | c.2014G>A |
| AA Mutation | p.Val672Ile(p.V672I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43877668:43877668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1795A>G |
| AA Mutation | p.Thr599Ala(p.T599A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43876674:43876674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750425699 |
| CDS Mutation | c.2789G>A |
| AA Mutation | p.Arg930Gln(p.R930Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43877875:43877875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1588C>T |
| AA Mutation | p.Arg530Trp(p.R530W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878087:43878087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1376G>A |
| AA Mutation | p.Gly459Asp(p.G459D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43876791:43876791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2672T>C |
| AA Mutation | p.Val891Ala(p.V891A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43877712:43877712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748860010 |
| CDS Mutation | c.1751A>G |
| AA Mutation | p.Gln584Arg(p.Q584R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878667:43878667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571911766 |
| CDS Mutation | c.796G>A |
| AA Mutation | p.Val266Met(p.V266M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43877553:43877553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1910C>A |
| AA Mutation | p.Pro637Gln(p.P637Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878715:43878715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.748T>C |
| AA Mutation | p.Phe250Leu(p.F250L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43876884:43876884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201901707 |
| CDS Mutation | c.2579G>A |
| AA Mutation | p.Arg860Gln(p.R860Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878967:43878967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.496G>A |
| AA Mutation | p.Ala166Thr(p.A166T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453200 |
| Start | 43877324:43877324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2139T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878272:43878272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453200 |
| Start | 43881923:43881923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563335497 |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878401:43878401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1062C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878551:43878551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.912C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453200 |
| Start | 43877462:43877462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369206269 |
| CDS Mutation | c.2001G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453200 |
| Start | 43878503:43878503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370165083 |
| CDS Mutation | c.960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |