Primary Site >> Stomach Cancer
Gene >> SMURF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361125 |
| Start | 99057446:99057446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.309T>G |
| AA Mutation | p.Asn103Lys(p.N103K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361125 |
| Start | 99049632:99049632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.962G>A |
| AA Mutation | p.Arg321Lys(p.R321K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361125 |
| Start | 99030675:99030675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2183G>A |
| AA Mutation | p.Arg728Gln(p.R728Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361125 |
| Start | 99049605:99049605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139427854 |
| CDS Mutation | c.989G>A |
| AA Mutation | p.Arg330Gln(p.R330Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361125 |
| Start | 99060636:99060636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166A>G |
| AA Mutation | p.Asn56Asp(p.N56D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000361125 |
| Start | 99057420:99057420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.335G>A |
| AA Mutation | p.Gly112Glu(p.G112E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361125 |
| Start | 99038468:99038468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1686C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361125 |
| Start | 99057457:99057457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.298C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361125 |
| Start | 99040527:99040527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771196252 |
| CDS Mutation | c.1479G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361125 |
| Start | 99052335:99052335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772861699 |
| CDS Mutation | c.591C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |