Primary Site >> Stomach Cancer
Gene >> CEACAM5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221992 |
| Start | 41715839:41715839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782807202 |
| CDS Mutation | c.893C>T |
| AA Mutation | p.Thr298Met(p.T298M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221992 |
| Start | 41715103:41715103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113097830 |
| CDS Mutation | c.557C>T |
| AA Mutation | p.Pro186Leu(p.P186L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221992 |
| Start | 41715727:41715727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140053609 |
| CDS Mutation | c.781G>A |
| AA Mutation | p.Ala261Thr(p.A261T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221992 |
| Start | 41721038:41721038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1888A>G |
| AA Mutation | p.Asn630Asp(p.N630D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221992 |
| Start | 41727263:41727263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2056G>A |
| AA Mutation | p.Gly686Arg(p.G686R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221992 |
| Start | 41718160:41718160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1270T>C |
| AA Mutation | p.Tyr424His(p.Y424H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221992 |
| Start | 41718307:41718307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376701458 |
| CDS Mutation | c.1417G>A |
| AA Mutation | p.Gly473Arg(p.G473R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221992 |
| Start | 41717636:41717636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781896194 |
| CDS Mutation | c.1140A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221992 |
| Start | 41721100:41721100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565105444 |
| CDS Mutation | c.1950C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221992 |
| Start | 41715702:41715702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.756G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221992 |
| Start | 41720977:41720977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782555811 |
| CDS Mutation | c.1827G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221992 |
| Start | 41720132:41720132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782644830 |
| CDS Mutation | c.1695C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000221992 |
| Start | 41715060:41715061(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.516_518dupGGA |
| AA Mutation | p.Gln172_Asp173insGlu(p.Q172_D173insE) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |