Primary Site >> Stomach Cancer
Gene >> SSTR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37206905:37206905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570846487 |
| CDS Mutation | c.899C>T |
| AA Mutation | p.Ala300Val(p.A300V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207245:37207245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779117007 |
| CDS Mutation | c.559G>A |
| AA Mutation | p.Gly187Ser(p.G187S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207593:37207593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.211C>T |
| AA Mutation | p.Arg71Trp(p.R71W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37206831:37206831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780770327 |
| CDS Mutation | c.973C>T |
| AA Mutation | p.Arg325Cys(p.R325C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207533:37207533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201547867 |
| CDS Mutation | c.271G>A |
| AA Mutation | p.Glu91Lys(p.E91K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37206807:37206807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375773160 |
| CDS Mutation | c.997C>T |
| AA Mutation | p.Arg333Cys(p.R333C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207680:37207680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777044647 |
| CDS Mutation | c.124G>A |
| AA Mutation | p.Val42Ile(p.V42I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207534:37207534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.270C>G |
| AA Mutation | p.Asp90Glu(p.D90E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207091:37207091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756595845 |
| CDS Mutation | c.713G>A |
| AA Mutation | p.Arg238His(p.R238H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610913 |
| Start | 37206964:37206964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770081383 |
| CDS Mutation | c.840C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207639:37207639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142559355 |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207213:37207213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.591G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207021:37207021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144127697 |
| CDS Mutation | c.783C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610913 |
| Start | 37207036:37207036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775912597 |
| CDS Mutation | c.768G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000610913 |
| Start | 37206581:37206582(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1222dupG |
| AA Mutation | p.Glu408GlyfsTer46(p.E408Gfs*46) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |