Revel Score:
ENST00000402655
0.015
ENST00000299644
0.015
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.79212064T>G , CM000678.2:g.79212064T>G | GRCh38 |
| NC_000016.9:g.79245961T>G , CM000678.1:g.79245961T>G | GRCh37 |
| NC_000016.8:g.77803462T>G | NCBI36 |
| NG_011698.1:g.1117411T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683929.1:c.*627T>G (WWOX) | ENSP00000507689.1:n.*627T>G | |
| ENST00000566780.6:c.*268T>G (WWOX) MANE Select | ENSP00000457230.1:n.*268T>G | |
| ENST00000402655.6:c.866T>G (WWOX) | ENSP00000384238.2:p.Val289Gly | |
| ENST00000406884.6:c.*268T>G (WWOX) | ENSP00000384495.2:n.*268T>G | |
| ENST00000539474.6:c.*300T>G (WWOX) | ENSP00000445210.2:n.*300T>G | |
| ENST00000566103.1:n.580T>G (WWOX) | ||
| ENST00000566780.5:c.*268T>G (WWOX) | ENSP00000457230.1:n.*268T>G | |
| ENST00000569332.5:c.*1310T>G (WWOX) | ENSP00000454788.1:n.*1310T>G | |
| NM_001291997.1:c.*268T>G (WWOX) | NP_001278926.1:n.*268T>G | |
| NM_016373.3:c.*268T>G (WWOX) | NP_057457.1:n.*268T>G | |
| XM_011523100.1:c.*268T>G (WWOX) | XP_011521402.1:n.*268T>G | |
| XM_011523103.3:c.*485T>G (WWOX) | XP_011521405.1:n.*485T>G | |
| XM_017023279.1:c.599T>G (WWOX) | XP_016878768.1:p.Val200Gly | |
| XM_024450279.1:c.*866A>C (MAF) | XP_024306047.1:n.*866A>C | |
| XR_001751902.2:n.4068A>C (MAF) | ||
| XR_002957802.1:n.4068A>C (MAF) | ||
| XR_002957803.1:n.4068A>C (MAF) | ||
| XR_002957804.1:n.4068A>C (MAF) | ||
| NM_016373.4:c.*268T>G (WWOX) MANE Select | NP_057457.1:n.*268T>G | |
| NM_001291997.2:c.*268T>G (WWOX) | NP_001278926.1:n.*268T>G |