Primary Site >> Stomach Cancer
Gene >> MTHFR
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000376590 |
| Start | 11794861:11794861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753278299 |
| CDS Mutation | c.1034G>A |
| AA Mutation | p.Arg345His(p.R345H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11801257:11801257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769381688 |
| CDS Mutation | c.379C>T |
| AA Mutation | p.His127Tyr(p.H127Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11792307:11792307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760886915 |
| CDS Mutation | c.1603C>T |
| AA Mutation | p.Arg535Trp(p.R535W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11801167:11801167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776195746 |
| CDS Mutation | c.469C>T |
| AA Mutation | p.Arg157Trp(p.R157W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11791221:11791221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770471347 |
| CDS Mutation | c.1738T>C |
| AA Mutation | p.Phe580Leu(p.F580L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11794055:11794055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777304472 |
| CDS Mutation | c.1382C>T |
| AA Mutation | p.Ala461Val(p.A461V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11794807:11794807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs786204023 |
| CDS Mutation | c.1088G>A |
| AA Mutation | p.Arg363His(p.R363H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11790852:11790852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1799A>C |
| AA Mutation | p.Glu600Ala(p.E600A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11796319:11796319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150847674 |
| CDS Mutation | c.667G>A |
| AA Mutation | p.Asp223Asn(p.D223N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376590 |
| Start | 11794732:11794732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769953411 |
| CDS Mutation | c.1163G>A |
| AA Mutation | p.Arg388His(p.R388H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376590 |
| Start | 11791291:11791291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778486116 |
| CDS Mutation | c.1668G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376590 |
| Start | 11790815:11790815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1836C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376590 |
| Start | 11801171:11801171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566125423 |
| CDS Mutation | c.465G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000376590 |
| Start | 11794823:11794823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377443637 |
| CDS Mutation | c.1072C>T |
| AA Mutation | p.Arg358Ter(p.R358*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000376590 |
| Start | 11800251:11800251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121434294 |
| CDS Mutation | c.547C>T |
| AA Mutation | p.Arg183Ter(p.R183*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |