| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274276 |
| Start |
38933252:38933252(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2748T>G |
| AA Mutation |
p.Asn916Lys(p.N916K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274276 |
| Start |
38881665:38881665(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.319T>C |
| AA Mutation |
p.Cys107Arg(p.C107R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000274276 |
| Start |
38923214:38923214(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1830T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |