| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314641 |
| Start |
105125482:105125482(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.448T>A |
| AA Mutation |
p.Cys150Ser(p.C150S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314641 |
| Start |
105116771:105116771(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.746T>G |
| AA Mutation |
p.Phe249Cys(p.F249C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000314641 |
| Start |
105124637:105124637(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.558A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |