| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372852 |
| Start |
39627019:39627019(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757763641
|
| CDS Mutation |
c.475G>A |
| AA Mutation |
p.Glu159Lys(p.E159K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000372852 |
| Start |
39627098:39627098(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.396G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000372852 |
| Start |
39639596:39639596(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.30C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |