Gene >> ID4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378700 |
| Start |
19837936:19837936(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.182C>T |
| AA Mutation |
p.Ala61Val(p.A61V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000378700 |
| Start |
19838070:19838070(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.316C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |