Gene >> PDE4B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329654 |
| Start |
66257675:66257675(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.505T>G |
| AA Mutation |
p.Phe169Val(p.F169V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329654 |
| Start |
66247491:66247491(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.313C>G |
| AA Mutation |
p.Arg105Gly(p.R105G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |