Gene >> HM13
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340852 |
| Start |
31566213:31566213(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.952G>A |
| AA Mutation |
p.Ala318Thr(p.A318T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000340852 |
| Start |
31538206:31538206(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.310C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |