Linked Data
ClinVar Variation Id:
1356028
dbSNP Id:
rs1484856529
gnomAD v3:
16-79211716-C-T
gnomAD v4:
16-79211716-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.79211716C>T , CM000678.2:g.79211716C>T | GRCh38 |
| NC_000016.9:g.79245613C>T , CM000678.1:g.79245613C>T | GRCh37 |
| NC_000016.8:g.77803114C>T | NCBI36 |
| NG_011698.1:g.1117063C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683929.1:c.*279C>T (WWOX) | ENSP00000507689.1:n.*279C>T | |
| ENST00000566780.6:c.1165C>T (WWOX) MANE Select | ENSP00000457230.1:p.Gln389Ter | |
| ENST00000402655.6:c.518C>T (WWOX) | ENSP00000384238.2:p.Ser173Leu | |
| ENST00000406884.6:c.625C>T (WWOX) | ENSP00000384495.2:p.Gln209Ter | |
| ENST00000539474.6:c.594C>T (WWOX) | ENSP00000445210.2:p.Leu198= | |
| ENST00000566103.1:n.232C>T (WWOX) | ||
| ENST00000566780.5:c.1165C>T (WWOX) | ENSP00000457230.1:p.Gln389Ter | |
| ENST00000569332.5:c.*962C>T (WWOX) | ENSP00000454788.1:n.*962C>T | |
| NM_001291997.1:c.826C>T (WWOX) | NP_001278926.1:p.Gln276Ter | |
| NM_016373.3:c.1165C>T (WWOX) | NP_057457.1:p.Gln389Ter | |
| XM_011523100.1:c.1261C>T (WWOX) | XP_011521402.1:p.Gln421Ter | |
| XM_011523103.3:c.*137C>T (WWOX) | XP_011521405.1:n.*137C>T | |
| XM_017023279.1:c.251C>T (WWOX) | XP_016878768.1:p.Ser84Leu | |
| XM_024450279.1:c.*1214G>A (MAF) | XP_024306047.1:n.*1214G>A | |
| XR_001751902.2:n.4416G>A (MAF) | ||
| XR_002957802.1:n.4416G>A (MAF) | ||
| XR_002957803.1:n.4416G>A (MAF) | ||
| XR_002957804.1:n.4416G>A (MAF) | ||
| NM_016373.4:c.1165C>T (WWOX) MANE Select | NP_057457.1:p.Gln389Ter | |
| NM_001291997.2:c.826C>T (WWOX) | NP_001278926.1:p.Gln276Ter |