| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282020 |
| Start |
93772106:93772106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2632C>T |
| AA Mutation |
p.His878Tyr(p.H878Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282020 |
| Start |
93224660:93224660(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1010C>A |
| AA Mutation |
p.Ala337Asp(p.A337D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000282020 |
| Start |
93085197:93085197(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.447T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |