Primary Site >> Stomach Cancer
Gene >> ABCG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42271127:42271127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.344C>T |
| AA Mutation | p.Ala115Val(p.A115V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42282397:42282397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712A>G |
| AA Mutation | p.Met238Val(p.M238V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42276898:42276898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.541T>C |
| AA Mutation | p.Ser181Pro(p.S181P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42291561:42291561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748557431 |
| CDS Mutation | c.1594G>A |
| AA Mutation | p.Val532Met(p.V532M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42282404:42282404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719T>C |
| AA Mutation | p.Phe240Ser(p.F240S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42287961:42287961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756353022 |
| CDS Mutation | c.1046G>A |
| AA Mutation | p.Cys349Tyr(p.C349Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42296342:42296342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1987C>T |
| AA Mutation | p.Arg663Cys(p.R663C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42291555:42291555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1588G>A |
| AA Mutation | p.Asp530Asn(p.D530N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42285991:42285991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.970T>G |
| AA Mutation | p.Phe324Val(p.F324V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42282356:42282356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.671G>A |
| AA Mutation | p.Arg224His(p.R224H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361802 |
| Start | 42294599:42294599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1747T>G |
| AA Mutation | p.Phe583Val(p.F583V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361802 |
| Start | 42285927:42285927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361802 |
| Start | 42296173:42296173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1818C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361802 |
| Start | 42284611:42284611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750833003 |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361802 |
| Start | 42296177:42296177(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1825delG |
| AA Mutation | p.Val609SerfsTer8(p.V609Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |