| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304748 |
| Start |
51746732:51746732(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.263G>T |
| AA Mutation |
p.Gly88Val(p.G88V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000304748 |
| Start |
51746491:51746491(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.504T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000304748 |
| Start |
51746674:51746674(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.321C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |