Revel Score:
ENST00000261584 (MANE Select)
0.027
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00001773 (EAS)
Genomes Max Group AF
0.00006825 (EAS)
Exomes Max Group AF
8.4e-7 (NFE)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23626376C>T , CM000678.2:g.23626376C>T | GRCh38 |
| NC_000016.9:g.23637697C>T , CM000678.1:g.23637697C>T | GRCh37 |
| NC_000016.8:g.23545198C>T | NCBI36 |
| NG_007406.1:g.19982G>A , LRG_308:g.19982G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.2614G>A | ENSP00000460666.3:p.Val872Ile | |
| ENST00000565038.2:c.*89G>A | ENSP00000459882.2:n.*89G>A | |
| ENST00000566069.6:c.2608G>A | ENSP00000459237.2:p.Val870Ile | |
| ENST00000697377.2:c.2593-2282G>A | ENSP00000513286.2:n.2593-2282G>A | |
| ENST00000697379.2:c.2614G>A | ENSP00000513287.2:p.Val872Ile | |
| ENST00000561514.2:c.1723G>A | ENSP00000460666.2:p.Val575Ile | |
| ENST00000697374.1:c.1723G>A | ENSP00000513284.1:p.Val575Ile | |
| ENST00000697375.1:n.3955G>A | ||
| ENST00000697376.1:c.1723G>A | ENSP00000513285.1:p.Val575Ile | |
| ENST00000697377.1:c.1702-2282G>A | ENSP00000513286.1:n.1702-2282G>A | |
| ENST00000697378.1:n.3128G>A | ||
| ENST00000697379.1:c.1723G>A | ENSP00000513287.1:p.Val575Ile | |
| ENST00000697380.1:n.1900G>A | ||
| ENST00000697381.1:n.1303G>A | ||
| ENST00000697382.1:c.1723G>A | ENSP00000513288.1:p.Val575Ile | |
| ENST00000697383.1:c.142G>A | ENSP00000513289.1:p.Val48Ile | |
| ENST00000261584.9:c.2608G>A MANE Select | ENSP00000261584.4:p.Val870Ile | |
| ENST00000261584.8:c.2608G>A | ENSP00000261584.4:p.Val870Ile | |
| ENST00000565038.1:c.180G>A | ||
| ENST00000568219.5:c.1723G>A | ENSP00000454703.2:p.Val575Ile | |
| NM_024675.3:c.2608G>A , LRG_308t1:c.2608G>A | NP_078951.2:p.Val870Ile | |
| XM_011545946.1:c.2614G>A | XP_011544248.1:p.Val872Ile | |
| XM_011545947.1:c.2614G>A | XP_011544249.1:p.Val872Ile | |
| XM_011545948.1:c.1723G>A | XP_011544250.1:p.Val575Ile | |
| XR_950851.1:n.3404G>A | ||
| XM_011545946.2:c.2614G>A | XP_011544248.1:p.Val872Ile | |
| XM_011545947.2:c.2614G>A | XP_011544249.1:p.Val872Ile | |
| XM_011545948.2:c.1723G>A | XP_011544250.1:p.Val575Ile | |
| XM_017023671.1:c.2614G>A | XP_016879160.1:p.Val872Ile | |
| XM_017023672.2:c.2608G>A | XP_016879161.1:p.Val870Ile | |
| XM_017023673.2:c.2608G>A | XP_016879162.1:p.Val870Ile | |
| NM_024675.4:c.2608G>A MANE Select | NP_078951.2:p.Val870Ile |