Primary Site >> Stomach Cancer
Gene >> GK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79407764:79407764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.437G>A |
| AA Mutation | p.Ser146Asn(p.S146N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79406943:79406943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267600273 |
| CDS Mutation | c.1258C>T |
| AA Mutation | p.Arg420Cys(p.R420C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79407995:79407995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752639242 |
| CDS Mutation | c.206C>T |
| AA Mutation | p.Ala69Val(p.A69V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79406984:79406984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1217A>G |
| AA Mutation | p.Glu406Gly(p.E406G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79407711:79407711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.490G>A |
| AA Mutation | p.Val164Ile(p.V164I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79407756:79407756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.445T>G |
| AA Mutation | p.Phe149Val(p.F149V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79406700:79406700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1501G>A |
| AA Mutation | p.Ala501Thr(p.A501T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79408076:79408076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.125A>C |
| AA Mutation | p.Glu42Ala(p.E42A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358842 |
| Start | 79408103:79408103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140376639 |
| CDS Mutation | c.98C>T |
| AA Mutation | p.Ala33Val(p.A33V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358842 |
| Start | 79407961:79407961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.240T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358842 |
| Start | 79407988:79407988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.213G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358842 |
| Start | 79406596:79406596(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1605delT |
| AA Mutation | p.Phe535LeufsTer2(p.F535Lfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358842 |
| Start | 79406595:79406596(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs752070089 |
| CDS Mutation | c.1605dupT |
| AA Mutation | p.Ile536TyrfsTer4(p.I536Yfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |