| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000290524 |
| Start |
151343124:151343124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764649554
|
| CDS Mutation |
c.913C>T |
| AA Mutation |
p.Arg305Trp(p.R305W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000290524 |
| Start |
151342606:151342606(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1431G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000290524 |
| Start |
151344233:151344233(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.519A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |