Primary Site >> Esophagus Cancer
Gene >> CCDC88A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436346 |
| Start | 55334966:55334966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1855C>T |
| AA Mutation | p.His619Tyr(p.H619Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436346 |
| Start | 55388879:55388879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.172A>C |
| AA Mutation | p.Lys58Gln(p.K58Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436346 |
| Start | 55317639:55317639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3527C>G |
| AA Mutation | p.Ser1176Cys(p.S1176C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436346 |
| Start | 55336716:55336716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1621A>T |
| AA Mutation | p.Thr541Ser(p.T541S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436346 |
| Start | 55296359:55296359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764420887 |
| CDS Mutation | c.4990C>G |
| AA Mutation | p.Leu1664Val(p.L1664V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436346 |
| Start | 55363971:55363971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374500852 |
| CDS Mutation | c.465G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000436346 |
| Start | 55301890:55301890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4654C>T |
| AA Mutation | p.Gln1552Ter(p.Q1552*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |