| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000346403 |
| Start |
24976330:24976330(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.181C>T |
| AA Mutation |
p.Arg61Cys(p.R61C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000346403 |
| Start |
24977847:24977847(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772663663
|
| CDS Mutation |
c.490G>T |
| AA Mutation |
p.Ala164Ser(p.A164S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000346403 |
| Start |
24978266:24978266(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372752818
|
| CDS Mutation |
c.633G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |