Gene >> ERCC5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355739 |
| Start |
102852142:102852142(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.113C>T |
| AA Mutation |
p.Ala38Val(p.A38V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000355739 |
| Start |
102862520:102862520(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149867583
|
| CDS Mutation |
c.1371C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |