Revel Score:
ENST00000359271 (MANE Select)
0.148
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00165199 (NFE)
Genomes Max Group AF
0.00135834 (NFE)
Exomes Max Group AF
0.00165687 (NFE)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46725551C>T , CM000682.2:g.46725551C>T | GRCh38 |
| NC_000020.10:g.45354190C>T , CM000682.1:g.45354190C>T | GRCh37 |
| NC_000020.9:g.44787597C>T | NCBI36 |
| NG_016284.1:g.20912C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359271.4:c.515C>T MANE Select | ENSP00000352216.2:p.Thr172Ile | |
| ENST00000359271.3:c.515C>T | ENSP00000352216.2:p.Thr172Ile | |
| NM_030777.3:c.515C>T | NP_110404.1:p.Thr172Ile | |
| XM_011529060.1:c.578C>T | XP_011527362.1:p.Thr193Ile | |
| XM_011529061.1:c.524C>T | XP_011527363.1:p.Thr175Ile | |
| XM_011529062.1:c.578C>T | XP_011527364.1:p.Thr193Ile | |
| XM_011529063.1:c.578C>T | XP_011527365.1:p.Thr193Ile | |
| XM_011529064.1:c.578C>T | XP_011527366.1:p.Thr193Ile | |
| XM_011529065.1:c.578C>T | XP_011527367.1:p.Thr193Ile | |
| XR_936641.1:n.714C>T | ||
| XM_011529060.2:c.578C>T | XP_011527362.1:p.Thr193Ile | |
| XM_011529061.2:c.524C>T | XP_011527363.1:p.Thr175Ile | |
| XM_011529062.2:c.578C>T | XP_011527364.1:p.Thr193Ile | |
| XM_011529063.2:c.578C>T | XP_011527365.1:p.Thr193Ile | |
| XM_011529064.2:c.578C>T | XP_011527366.1:p.Thr193Ile | |
| XM_011529065.2:c.578C>T | XP_011527367.1:p.Thr193Ile | |
| XM_017028087.2:c.515C>T | XP_016883576.1:p.Thr172Ile | |
| XR_936641.2:n.701C>T | ||
| NM_030777.4:c.515C>T MANE Select | NP_110404.1:p.Thr172Ile |