| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304725 |
| Start |
23825277:23825277(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.275C>A |
| AA Mutation |
p.Thr92Asn(p.T92N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304725 |
| Start |
23826465:23826465(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs112783512
|
| CDS Mutation |
c.196C>T |
| AA Mutation |
p.Arg66Cys(p.R66C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000304725 |
| Start |
23824029:23824029(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.417A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |