Primary Site >> Stomach Cancer
Gene >> HGFAC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3447569:3447569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1433G>A |
| AA Mutation | p.Gly478Asp(p.G478D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3448181:3448181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767158380 |
| CDS Mutation | c.1690G>A |
| AA Mutation | p.Asp564Asn(p.D564N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3447574:3447574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750501405 |
| CDS Mutation | c.1438G>A |
| AA Mutation | p.Glu480Lys(p.E480K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3442093:3442093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748796749 |
| CDS Mutation | c.92G>A |
| AA Mutation | p.Arg31Gln(p.R31Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3444650:3444650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.758G>A |
| AA Mutation | p.Gly253Glu(p.G253E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3447969:3447969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557582250 |
| CDS Mutation | c.1570G>A |
| AA Mutation | p.Glu524Lys(p.E524K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3443101:3443101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554424799 |
| CDS Mutation | c.350G>A |
| AA Mutation | p.Arg117His(p.R117H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3444086:3444086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523T>C |
| AA Mutation | p.Cys175Arg(p.C175R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3449252:3449252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775128737 |
| CDS Mutation | c.1801C>G |
| AA Mutation | p.Pro601Ala(p.P601A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382774 |
| Start | 3449349:3449349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374846787 |
| CDS Mutation | c.1898G>A |
| AA Mutation | p.Arg633His(p.R633H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382774 |
| Start | 3442070:3442070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538844201 |
| CDS Mutation | c.69C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382774 |
| Start | 3446169:3446169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373005235 |
| CDS Mutation | c.1230C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382774 |
| Start | 3444666:3444666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.774G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382774 |
| Start | 3444354:3444354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762054716 |
| CDS Mutation | c.642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382774 |
| Start | 3444384:3444384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372890331 |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382774 |
| Start | 3447594:3447594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1458C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382774 |
| Start | 3449246:3449246(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774180159 |
| CDS Mutation | c.1800delG |
| AA Mutation | p.Leu602TrpfsTer70(p.L602Wfs*70) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000382774 |
| Start | 3447492:3447492(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761929917 |
| CDS Mutation | c.1362delC |
| AA Mutation | p.Arg455GlyfsTer19(p.R455Gfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382774 |
| Start | 3444127:3444127(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.568delC |
| AA Mutation | p.Arg190GlyfsTer57(p.R190Gfs*57) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000382774 |
| Start | 3447491:3447492(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs777027535 |
| CDS Mutation | c.1362dupC |
| AA Mutation | p.Arg455GlnfsTer91(p.R455Qfs*91) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |