Gene >> FANCC
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000289081 |
| Start |
95117350:95117350(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1037C>T |
| AA Mutation |
p.Pro346Leu(p.P346L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000289081 |
| Start |
95101732:95101732(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1652T>C |
| AA Mutation |
p.Leu551Pro(p.L551P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |