| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000519560 |
| Start |
168817309:168817309(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.784G>A |
| AA Mutation |
p.Val262Met(p.V262M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000519560 |
| Start |
168685780:168685780(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767305316
|
| CDS Mutation |
c.3462C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000519560 |
| Start |
168712342:168712342(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2496C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |