| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000521059 |
| Start |
140735395:140735395(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1886A>G |
| AA Mutation |
p.Asn629Ser(p.N629S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000521059 |
| Start |
140864357:140864357(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.405C>G |
| AA Mutation |
p.Asn135Lys(p.N135K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000521059 |
| Start |
140706167:140706167(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2181A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |