| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000450114 |
| Start |
9585269:9585269(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs147537355
|
| CDS Mutation |
c.1300A>G |
| AA Mutation |
p.Ile434Val(p.I434V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000450114 |
| Start |
9576244:9576244(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.797A>G |
| AA Mutation |
p.Asp266Gly(p.D266G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000450114 |
| Start |
9576237:9576237(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.790G>A |
| AA Mutation |
p.Gly264Ser(p.G264S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |