| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339252 |
| Start |
157052634:157052634(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs181065847
|
| CDS Mutation |
c.400A>G |
| AA Mutation |
p.Ile134Val(p.I134V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339252 |
| Start |
157055249:157055249(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.331G>A |
| AA Mutation |
p.Gly111Arg(p.G111R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000339252 |
| Start |
157052614:157052614(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs566987531
|
| CDS Mutation |
c.420C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |