| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000247452 |
| Start |
142203160:142203160(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.828A>C |
| AA Mutation |
p.Lys276Asn(p.K276N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000247452 |
| Start |
142203110:142203110(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.878C>T |
| AA Mutation |
p.Ser293Phe(p.S293F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000247452 |
| Start |
142203106:142203106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.882T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |