Primary Site >> Stomach Cancer
Gene >> H6PD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377403 |
| Start | 9246982:9246982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.644T>C |
| AA Mutation | p.Leu215Pro(p.L215P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377403 |
| Start | 9245439:9245439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35668164 |
| CDS Mutation | c.505C>T |
| AA Mutation | p.Arg169Trp(p.R169W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377403 |
| Start | 9245205:9245205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.271G>A |
| AA Mutation | p.Ala91Thr(p.A91T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377403 |
| Start | 9264132:9264132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1639A>G |
| AA Mutation | p.Arg547Gly(p.R547G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377403 |
| Start | 9244995:9244995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.61G>A |
| AA Mutation | p.Glu21Lys(p.E21K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377403 |
| Start | 9244978:9244978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.44G>A |
| AA Mutation | p.Gly15Asp(p.G15D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377403 |
| Start | 9245324:9245324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.390C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377403 |
| Start | 9245429:9245429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143453022 |
| CDS Mutation | c.495C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377403 |
| Start | 9245468:9245468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.534T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377403 |
| Start | 9262226:9262226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.913A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377403 |
| Start | 9264645:9264645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554286034 |
| CDS Mutation | c.2152C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377403 |
| Start | 9264851:9264851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531681724 |
| CDS Mutation | c.2358C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377403 |
| Start | 9263806:9263806(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1316delT |
| AA Mutation | p.Phe439SerfsTer125(p.F439Sfs*125) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000377403 |
| Start | 9264144:9264144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760131543 |
| CDS Mutation | c.1651C>T |
| AA Mutation | p.Arg551Ter(p.R551*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |