Gene >> CTLA4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302823 |
| Start |
203868003:203868003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.61C>A |
| AA Mutation |
p.Pro21Thr(p.P21T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302823 |
| Start |
203871388:203871388(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200657280
|
| CDS Mutation |
c.468G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |