| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000610913 |
| Start |
37207050:37207050(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.754G>A |
| AA Mutation |
p.Glu252Lys(p.E252K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000610913 |
| Start |
37206857:37206857(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.947T>G |
| AA Mutation |
p.Leu316Arg(p.L316R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000610913 |
| Start |
37207051:37207051(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.753C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |