| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000297350 |
| Start |
118924649:118924649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.931G>C |
| AA Mutation |
p.Asp311His(p.D311H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000297350 |
| Start |
118924759:118924759(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.821T>A |
| AA Mutation |
p.Ile274Asn(p.I274N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000297350 |
| Start |
118924393:118924393(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1187T>G |
| AA Mutation |
p.Val396Gly(p.V396G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |