| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000404115 |
| Start |
120540389:120540389(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1671T>G |
| AA Mutation |
p.Asn557Lys(p.N557K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000404115 |
| Start |
120540552:120540552(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1508G>T |
| AA Mutation |
p.Ser503Ile(p.S503I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000404115 |
| Start |
120534548:120534548(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2253G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |