| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301012 |
| Start |
88657495:88657495(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.344T>C |
| AA Mutation |
p.Val115Ala(p.V115A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301012 |
| Start |
88654797:88654797(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.908C>T |
| AA Mutation |
p.Thr303Ile(p.T303I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000301012 |
| Start |
88655707:88655707(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.627A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |