Primary Site >> Stomach Cancer
Gene >> MC3R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249487:56249487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.644G>A |
| AA Mutation | p.Arg215Gln(p.R215Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249289:56249289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552943206 |
| CDS Mutation | c.446C>T |
| AA Mutation | p.Ala149Val(p.A149V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249762:56249762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.919C>T |
| AA Mutation | p.Arg307Cys(p.R307C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249763:56249763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.920G>A |
| AA Mutation | p.Arg307His(p.R307H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249363:56249363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.520G>A |
| AA Mutation | p.Val174Ile(p.V174I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249136:56249136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.293T>A |
| AA Mutation | p.Ile98Asn(p.I98N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56248913:56248913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.70C>T |
| AA Mutation | p.Pro24Ser(p.P24S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249384:56249384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778979632 |
| CDS Mutation | c.541G>A |
| AA Mutation | p.Val181Ile(p.V181I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249252:56249252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.409G>A |
| AA Mutation | p.Ala137Thr(p.A137T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249544:56249544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701A>G |
| AA Mutation | p.Gln234Arg(p.Q234R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249669:56249669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.826T>A |
| AA Mutation | p.Cys276Ser(p.C276S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249524:56249524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.681C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249257:56249257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.414C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249371:56249371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749544417 |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249044:56249044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.201C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249287:56249287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147084433 |
| CDS Mutation | c.444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249041:56249041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.198C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249359:56249359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243911 |
| Start | 56249398:56249398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772955913 |
| CDS Mutation | c.555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |