Primary Site >> Stomach Cancer
Gene >> BRCA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43091783:43091783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28897686 |
| CDS Mutation | c.3748G>A |
| AA Mutation | p.Glu1250Lys(p.E1250K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43092836:43092836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2695G>C |
| AA Mutation | p.Val899Leu(p.V899L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43092872:43092872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2659G>A |
| AA Mutation | p.Ala887Thr(p.A887T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43074510:43074510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4496C>T |
| AA Mutation | p.Ser1499Phe(p.S1499F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43094428:43094428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1103A>G |
| AA Mutation | p.Glu368Gly(p.E368G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43082571:43082571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4190G>T |
| AA Mutation | p.Arg1397Met(p.R1397M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43092560:43092560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2971A>C |
| AA Mutation | p.Lys991Gln(p.K991Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43093702:43093702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1829G>T |
| AA Mutation | p.Arg610Met(p.R610M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43093946:43093946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769380445 |
| CDS Mutation | c.1585C>T |
| AA Mutation | p.Pro529Ser(p.P529S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43092852:43092852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587781771 |
| CDS Mutation | c.2679G>T |
| AA Mutation | p.Lys893Asn(p.K893N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43092449:43092449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80357049 |
| CDS Mutation | c.3082C>T |
| AA Mutation | p.Arg1028Cys(p.R1028C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357654 |
| Start | 43091758:43091758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3773A>G |
| AA Mutation | p.Glu1258Gly(p.E1258G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000357654 |
| Start | 43067608:43067608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80187739 |
| CDS Mutation | c.5074G>A |
| AA Mutation | p.Asp1692Asn(p.D1692N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357654 |
| Start | 43104938:43104938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80356847 |
| CDS Mutation | c.231G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357654 |
| Start | 43076532:43076532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4440T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357654 |
| Start | 43093743:43093743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779253414 |
| CDS Mutation | c.1788C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000357654 |
| Start | 43057078:43057078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80357123 |
| CDS Mutation | c.5251C>T |
| AA Mutation | p.Arg1751Ter(p.R1751*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000357654 |
| Start | 43093689:43093690(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1841_1842insTCACTGTCAT |
| AA Mutation | p.Lys614AsnfsTer14(p.K614Nfs*14) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |