Primary Site >> Stomach Cancer
Gene >> CHAT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49619755:49619755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.418C>A |
| AA Mutation | p.Gln140Lys(p.Q140K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49655422:49655422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1813C>T |
| AA Mutation | p.Arg605Cys(p.R605C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49664931:49664931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2132T>C |
| AA Mutation | p.Val711Ala(p.V711A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49619770:49619770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.433A>G |
| AA Mutation | p.Thr145Ala(p.T145A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49651895:49651895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1523A>C |
| AA Mutation | p.Asn508Thr(p.N508T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49646601:49646601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1208G>T |
| AA Mutation | p.Arg403Met(p.R403M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49655158:49655158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760452753 |
| CDS Mutation | c.1698C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49622124:49622124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.726A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49655122:49655122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145370753 |
| CDS Mutation | c.1662C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49625563:49625563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.843G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49627736:49627736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529337162 |
| CDS Mutation | c.1062G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49649608:49649608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1483T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49646590:49646590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554276268 |
| CDS Mutation | c.1197C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49622115:49622115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.717C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000337653 |
| Start | 49619826:49619826(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.490delG |
| AA Mutation | p.Ala164ProfsTer36(p.A164Pfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000337653 |
| Start | 49649533:49649533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142889639 |
| CDS Mutation | c.1408C>T |
| AA Mutation | p.Arg470Ter(p.R470*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |