| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000232014 |
| Start |
187731743:187731743(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.349G>T |
| AA Mutation |
p.Val117Phe(p.V117F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000232014 |
| Start |
187729892:187729892(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751896144
|
| CDS Mutation |
c.513C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000232014 |
| Start |
187728412:187728412(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370060611
|
| CDS Mutation |
c.1488G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |