| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357266 |
| Start |
35619143:35619143(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140297532
|
| CDS Mutation |
c.461G>A |
| AA Mutation |
p.Arg154Gln(p.R154Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357266 |
| Start |
35580215:35580215(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.847A>G |
| AA Mutation |
p.Lys283Glu(p.K283E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357266 |
| Start |
35580135:35580135(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764691592
|
| CDS Mutation |
c.927G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |