| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357639 |
| Start |
131746888:131746888(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2560A>G |
| AA Mutation |
p.Lys854Glu(p.K854E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357639 |
| Start |
131675099:131675099(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776096391
|
| CDS Mutation |
c.782A>G |
| AA Mutation |
p.Tyr261Cys(p.Y261C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357639 |
| Start |
131685422:131685422(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1179A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |