Primary Site >> Stomach Cancer
Gene >> INSRR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156845091:156845091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756026000 |
| CDS Mutation | c.2422C>T |
| AA Mutation | p.Arg808Cys(p.R808C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156853887:156853887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752601283 |
| CDS Mutation | c.502G>A |
| AA Mutation | p.Val168Met(p.V168M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156852135:156852135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140347940 |
| CDS Mutation | c.694G>A |
| AA Mutation | p.Glu232Lys(p.E232K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156841752:156841752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3440G>A |
| AA Mutation | p.Arg1147His(p.R1147H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156851987:156851987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.842C>T |
| AA Mutation | p.Ala281Val(p.A281V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156844251:156844251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2767C>A |
| AA Mutation | p.Leu923Ile(p.L923I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156852122:156852122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707G>T |
| AA Mutation | p.Gly236Val(p.G236V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156849434:156849434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1256A>G |
| AA Mutation | p.Asn419Ser(p.N419S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156841496:156841496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755019469 |
| CDS Mutation | c.3560C>T |
| AA Mutation | p.Thr1187Ile(p.T1187I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156844478:156844478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2721C>G |
| AA Mutation | p.Phe907Leu(p.F907L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368195 |
| Start | 156843194:156843194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2936T>A |
| AA Mutation | p.Ile979Asn(p.I979N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368195 |
| Start | 156849262:156849262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549652989 |
| CDS Mutation | c.1428C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368195 |
| Start | 156854122:156854122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs62640942 |
| CDS Mutation | c.267C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368195 |
| Start | 156844221:156844221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2797C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368195 |
| Start | 156846745:156846745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368851308 |
| CDS Mutation | c.1584C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368195 |
| Start | 156842401:156842401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3234A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368195 |
| Start | 156854149:156854149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149908610 |
| CDS Mutation | c.240C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368195 |
| Start | 156849270:156849270(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1420delC |
| AA Mutation | p.Arg474AlafsTer20(p.R474Afs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368195 |
| Start | 156852122:156852122(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.707delG |
| AA Mutation | p.Gly236AlafsTer12(p.G236Afs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368195 |
| Start | 156844575:156844575(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2624delG |
| AA Mutation | p.Gly875GlufsTer82(p.G875Efs*82) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368195 |
| Start | 156852042:156852048(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.781_787delGCCTGCC |
| AA Mutation | p.Ala261ArgfsTer68(p.A261Rfs*68) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368195 |
| Start | 156845249:156845249(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2264delG |
| AA Mutation | p.Gly755AlafsTer20(p.G755Afs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368195 |
| Start | 156846564:156846564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772428423 |
| CDS Mutation | c.1765C>T |
| AA Mutation | p.Gln589Ter(p.Q589*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |