| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000410059 |
| Start |
115525907:115525907(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.376A>G |
| AA Mutation |
p.Lys126Glu(p.K126E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000410059 |
| Start |
115753212:115753212(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.989C>A |
| AA Mutation |
p.Thr330Asn(p.T330N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000410059 |
| Start |
115309256:115309256(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.78C>A |
| AA Mutation |
p.Ser26Arg(p.S26R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |