| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292928 |
| Start |
36627477:36627477(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1580A>G |
| AA Mutation |
p.Lys527Arg(p.K527R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292928 |
| Start |
36626792:36626792(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.895C>G |
| AA Mutation |
p.Pro299Ala(p.P299A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000292928 |
| Start |
36627022:36627022(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148103215
|
| CDS Mutation |
c.1125G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |