Gene >> FANCC
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000289081 |
| Start |
95249180:95249180(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.112G>T |
| AA Mutation |
p.Val38Leu(p.V38L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000289081 |
| Start |
95107237:95107237(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1362G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |