| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256594 |
| Start |
109737684:109737684(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.440G>A |
| AA Mutation |
p.Gly147Glu(p.G147E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256594 |
| Start |
109738300:109738300(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs557438670
|
| CDS Mutation |
c.256C>T |
| AA Mutation |
p.Arg86Cys(p.R86C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256594 |
| Start |
109737719:109737719(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.405A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |