| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305476 |
| Start |
96861303:96861303(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1825C>A |
| AA Mutation |
p.Leu609Ile(p.L609I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305476 |
| Start |
96864028:96864028(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1228C>T |
| AA Mutation |
p.Arg410Cys(p.R410C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305476 |
| Start |
96861406:96861406(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1722G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |