Gene >> CCDC3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378825 |
| Start |
12998480:12998480(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.407G>T |
| AA Mutation |
p.Gly136Val(p.G136V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378825 |
| Start |
12998436:12998436(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.451A>G |
| AA Mutation |
p.Arg151Gly(p.R151G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |