Primary Site >> Stomach Cancer
Gene >> CYP19A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51215773:51215773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.788G>T |
| AA Mutation | p.Arg263Ile(p.R263I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51212460:51212460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121434536 |
| CDS Mutation | c.1123C>T |
| AA Mutation | p.Arg375Cys(p.R375C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51212414:51212414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1169A>G |
| AA Mutation | p.Lys390Arg(p.K390R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51215214:51215214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.877A>G |
| AA Mutation | p.Arg293Gly(p.R293G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51222501:51222501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76174961 |
| CDS Mutation | c.476G>A |
| AA Mutation | p.Arg159His(p.R159H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51212490:51212490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202076619 |
| CDS Mutation | c.1093C>T |
| AA Mutation | p.Arg365Trp(p.R365W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51222403:51222403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.574C>T |
| AA Mutation | p.Arg192Cys(p.R192C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51210974:51210974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1346C>T |
| AA Mutation | p.Ala449Val(p.A449V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260433 |
| Start | 51210988:51210988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1332G>A |
| AA Mutation | p.Met444Ile(p.M444I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260433 |
| Start | 51210871:51210871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1449G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260433 |
| Start | 51222419:51222419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767683305 |
| CDS Mutation | c.558C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260433 |
| Start | 51210862:51210862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1458C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260433 |
| Start | 51236868:51236869(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.286_287delAT |
| AA Mutation | p.Ile96TyrfsTer33(p.I96Yfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260433 |
| Start | 51212405:51212405(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1178delA |
| AA Mutation | p.Asn393ThrfsTer4(p.N393Tfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260433 |
| Start | 51210951:51210951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs72552260 |
| CDS Mutation | c.1369C>T |
| AA Mutation | p.Arg457Ter(p.R457*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |