| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252997 |
| Start |
62465387:62465387(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.991C>A |
| AA Mutation |
p.Pro331Thr(p.P331T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252997 |
| Start |
62473473:62473473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.629G>A |
| AA Mutation |
p.Cys210Tyr(p.C210Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000252997 |
| Start |
62465883:62465883(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.864G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |