| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000392271 |
| Start |
30005439:30005439(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.446A>G |
| AA Mutation |
p.Gln149Arg(p.Q149R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392271 |
| Start |
30012513:30012513(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1407C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392271 |
| Start |
30014994:30014994(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1533T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |