| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000321867 |
| Start |
131908739:131908739(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.412G>A |
| AA Mutation |
p.Asp138Asn(p.D138N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000321867 |
| Start |
131909975:131909975(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377295019
|
| CDS Mutation |
c.782G>A |
| AA Mutation |
p.Arg261His(p.R261H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000321867 |
| Start |
131921352:131921352(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3144C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |