Gene >> CAP2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229922 |
| Start |
17513898:17513898(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.580G>C |
| AA Mutation |
p.Glu194Gln(p.E194Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000229922 |
| Start |
17463028:17463028(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.255G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |