| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296795 |
| Start |
186083440:186083440(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1754T>C |
| AA Mutation |
p.Leu585Ser(p.L585S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296795 |
| Start |
186077041:186077041(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.422A>G |
| AA Mutation |
p.Asn141Ser(p.N141S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296795 |
| Start |
186076754:186076754(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.135A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |