| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000289547 |
| Start |
44540076:44540076(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.321G>T |
| AA Mutation |
p.Lys107Asn(p.K107N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000289547 |
| Start |
44540305:44540305(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.92G>A |
| AA Mutation |
p.Gly31Asp(p.G31D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000289547 |
| Start |
44522237:44522237(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770546328
|
| CDS Mutation |
c.2643G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |