Revel Score:
ENST00000226279 (MANE Select)
0.140
ENST00000510674
0.140
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00900728 (EAS)
Genomes Max Group AF
0.00224447 (EAS)
Exomes Max Group AF
0.00974734 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.15824935C>T , CM000666.2:g.15824935C>T | GRCh38 |
| NC_000004.11:g.15826558C>T , CM000666.1:g.15826558C>T | GRCh37 |
| NC_000004.10:g.15435656C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226279.8:c.418C>T MANE Select | ENSP00000226279.2:p.Arg140Trp | |
| ENST00000226279.7:c.418C>T | ENSP00000226279.2:p.Arg140Trp | |
| ENST00000502843.5:c.363+8295C>T | ENSP00000427277.1:n.363+8295C>T | |
| ENST00000510674.1:c.100C>T | ENSP00000423047.1:p.Arg34Trp | |
| ENST00000511430.1:n.521C>T | ||
| NM_001775.2:c.418C>T | NP_001766.2:p.Arg140Trp | |
| NM_001775.3:c.418C>T | NP_001766.2:p.Arg140Trp | |
| NR_132660.1:n.513+8295C>T | ||
| XR_241678.1:n.535C>T | ||
| NM_001775.4:c.418C>T MANE Select | NP_001766.2:p.Arg140Trp | |
| NR_132660.2:n.450+8295C>T |