Primary Site >> Stomach Cancer
Gene >> EHMT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137754259:137754259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745964626 |
| CDS Mutation | c.1337G>A |
| AA Mutation | p.Arg446Gln(p.R446Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137817482:137817482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3418G>A |
| AA Mutation | p.Val1140Met(p.V1140M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137716814:137716814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274G>A |
| AA Mutation | p.Ala92Thr(p.A92T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137782353:137782353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2338G>A |
| AA Mutation | p.Ala780Thr(p.A780T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137752397:137752397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1237G>A |
| AA Mutation | p.Glu413Lys(p.E413K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137776828:137776828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758755536 |
| CDS Mutation | c.2002G>A |
| AA Mutation | p.Asp668Asn(p.D668N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137777886:137777886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2023G>A |
| AA Mutation | p.Ala675Thr(p.A675T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137716769:137716769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768764806 |
| CDS Mutation | c.229G>A |
| AA Mutation | p.Ala77Thr(p.A77T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137815984:137815984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3296C>T |
| AA Mutation | p.Pro1099Leu(p.P1099L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137817462:137817462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754986694 |
| CDS Mutation | c.3398C>T |
| AA Mutation | p.Thr1133Met(p.T1133M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137777991:137777991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs398124403 |
| CDS Mutation | c.2128G>A |
| AA Mutation | p.Gly710Ser(p.G710S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000460843 |
| Start | 137790849:137790849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2384C>T |
| AA Mutation | p.Ala795Val(p.A795V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137834392:137834392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3584T>C |
| AA Mutation | p.Val1195Ala(p.V1195A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137834496:137834496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61744215 |
| CDS Mutation | c.3688C>T |
| AA Mutation | p.Arg1230Cys(p.R1230C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137834849:137834849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3793C>T |
| AA Mutation | p.His1265Tyr(p.H1265Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137790867:137790867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2402C>T |
| AA Mutation | p.Thr801Ile(p.T801I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137775203:137775203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1742G>A |
| AA Mutation | p.Arg581His(p.R581H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460843 |
| Start | 137778039:137778039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2176G>A |
| AA Mutation | p.Ala726Thr(p.A726T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137716690:137716690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371344592 |
| CDS Mutation | c.150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137716945:137716945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200982880 |
| CDS Mutation | c.405G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137743997:137743997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189753830 |
| CDS Mutation | c.1077C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137779686:137779686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2244A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137776701:137776701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1875C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137743988:137743988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1068C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137800885:137800885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755544597 |
| CDS Mutation | c.2613C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137752336:137752336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373083497 |
| CDS Mutation | c.1176C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460843 |
| Start | 137813431:137813431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777106945 |
| CDS Mutation | c.3081C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |