| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254227 |
| Start |
26913649:26913649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.292C>A |
| AA Mutation |
p.Leu98Ile(p.L98I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254227 |
| Start |
26913850:26913850(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.91G>A |
| AA Mutation |
p.Ala31Thr(p.A31T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254227 |
| Start |
26911967:26911967(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.652C>G |
| AA Mutation |
p.Leu218Val(p.L218V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |