| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306897 |
| Start |
82033804:82033804(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760585885
|
| CDS Mutation |
c.554C>T |
| AA Mutation |
p.Pro185Leu(p.P185L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306897 |
| Start |
82033455:82033455(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775842656
|
| CDS Mutation |
c.304C>T |
| AA Mutation |
p.Arg102Trp(p.R102W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000306897 |
| Start |
82033787:82033787(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs556605529
|
| CDS Mutation |
c.537G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |