| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261891 |
| Start |
63912113:63912113(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.943T>A |
| AA Mutation |
p.Trp315Arg(p.W315R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261891 |
| Start |
63983678:63983678(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs773075712
|
| CDS Mutation |
c.169C>T |
| AA Mutation |
p.Arg57Trp(p.R57W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261891 |
| Start |
63983665:63983665(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.182C>A |
| AA Mutation |
p.Ala61Glu(p.A61E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |