Gene >> GIT2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355312 |
| Start |
109947429:109947429(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1468T>C |
| AA Mutation |
p.Ser490Pro(p.S490P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000355312 |
| Start |
109959857:109959857(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1089G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |