| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357422 |
| Start |
46266095:46266095(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.937C>T |
| AA Mutation |
p.Arg313Cys(p.R313C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357422 |
| Start |
46266089:46266089(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.931T>A |
| AA Mutation |
p.Tyr311Asn(p.Y311N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357422 |
| Start |
46266088:46266088(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.930G>T |
| AA Mutation |
p.Lys310Asn(p.K310N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |