| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000303221 |
| Start |
50399878:50399878(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.947T>C |
| AA Mutation |
p.Val316Ala(p.V316A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303221 |
| Start |
50403392:50403392(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.663G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303221 |
| Start |
50405746:50405746(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.579C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |