| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264335 |
| Start |
1354337:1354337(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.589G>A |
| AA Mutation |
p.Ala197Thr(p.A197T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264335 |
| Start |
1361273:1361273(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.397G>A |
| AA Mutation |
p.Ala133Thr(p.A133T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264335 |
| Start |
1400079:1400079(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777592060
|
| CDS Mutation |
c.32C>T |
| AA Mutation |
p.Ala11Val(p.A11V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |