| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000539798 |
| Start |
75429824:75429824(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.806G>A |
| AA Mutation |
p.Arg269His(p.R269H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000539798 |
| Start |
75425486:75425486(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1281C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000539798 |
| Start |
75428593:75428593(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.915C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |