| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285930 |
| Start |
134451708:134451708(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748304576
|
| CDS Mutation |
c.112G>A |
| AA Mutation |
p.Val38Ile(p.V38I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285930 |
| Start |
134448422:134448422(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372432846
|
| CDS Mutation |
c.624C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285930 |
| Start |
134450798:134450798(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs199863988
|
| CDS Mutation |
c.339G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |