Primary Site >> Stomach Cancer
Gene >> MC1R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000555147 |
| Start | 89920036:89920036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778C>T |
| AA Mutation | p.His260Tyr(p.H260Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000555147 |
| Start | 89919895:89919895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200000734 |
| CDS Mutation | c.637C>T |
| AA Mutation | p.Arg213Trp(p.R213W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000555147 |
| Start | 89919475:89919475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371458749 |
| CDS Mutation | c.217A>G |
| AA Mutation | p.Met73Val(p.M73V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000555147 |
| Start | 89919944:89919944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376780075 |
| CDS Mutation | c.686G>A |
| AA Mutation | p.Arg229His(p.R229H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000555147 |
| Start | 89919871:89919871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749525002 |
| CDS Mutation | c.613G>A |
| AA Mutation | p.Val205Met(p.V205M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000555147 |
| Start | 89920096:89920096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.838T>C |
| AA Mutation | p.Phe280Leu(p.F280L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000555147 |
| Start | 89919869:89919869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611C>T |
| AA Mutation | p.Ala204Val(p.A204V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000555147 |
| Start | 89919522:89919522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767294514 |
| CDS Mutation | c.264C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000555147 |
| Start | 89919675:89919675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372929572 |
| CDS Mutation | c.417C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |