| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265724 |
| Start |
87520852:87520852(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2710T>G |
| AA Mutation |
p.Phe904Val(p.F904V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265724 |
| Start |
87566855:87566855(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.460G>T |
| AA Mutation |
p.Ala154Ser(p.A154S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265724 |
| Start |
87531481:87531481(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2498T>C |
| AA Mutation |
p.Leu833Pro(p.L833P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |