| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000200181 |
| Start |
75742658:75742658(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2859G>C |
| AA Mutation |
p.Glu953Asp(p.E953D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000200181 |
| Start |
75755833:75755833(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.4691A>G |
| AA Mutation |
p.Tyr1564Cys(p.Y1564C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000200181 |
| Start |
75753781:75753781(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4125C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |