Gene >> SFTPA1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000398636 |
| Start |
79612428:79612428(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.289C>A |
| AA Mutation |
p.Pro97Thr(p.P97T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000398636 |
| Start |
79613962:79613962(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.596G>C |
| AA Mutation |
p.Arg199Pro(p.R199P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |