| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262410 |
| Start |
45983598:45983598(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.794T>A |
| AA Mutation |
p.Ile265Asn(p.I265N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262410 |
| Start |
45974445:45974445(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.281A>G |
| AA Mutation |
p.His94Arg(p.H94R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262410 |
| Start |
45996481:45996481(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201157234
|
| CDS Mutation |
c.1590G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |