Linked Data
ClinVar Variation Id:
354182
ClinVar RCV Id:
RCV000284949
dbSNP Id:
rs886060762
gnomAD v4:
5-77426841-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.77426841C>T , CM000667.2:g.77426841C>T | GRCh38 |
| NC_000005.9:g.76722666C>T , CM000667.1:g.76722666C>T | GRCh37 |
| NC_000005.8:g.76758422C>T | NCBI36 |
| NG_023364.1:g.220961C>T | |
| NG_023364.2:g.251590C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264917.10:c.*287C>T (PDE8B) MANE Select | ENSP00000264917.6:n.*287C>T | |
| ENST00000646262.1:c.*287C>T | ENSP00000493971.1:n.*287C>T | |
| ENST00000264917.9:c.*287C>T (PDE8B) | ENSP00000264917.5:n.*287C>T | |
| ENST00000340978.7:c.*287C>T (PDE8B) | ENSP00000345446.3:n.*287C>T | |
| ENST00000346042.7:c.*287C>T (PDE8B) | ENSP00000330428.3:n.*287C>T | |
| ENST00000505283.1:c.*287C>T (PDE8B) | ENSP00000423461.1:n.*287C>T | |
| ENST00000508154.1:n.269G>A (WDR41) | ||
| ENST00000512033.1:n.608G>A (WDR41) | ||
| ENST00000514878.1:n.154+103G>A (WDR41) | ||
| NM_001029851.2:c.*287C>T (PDE8B) | NP_001025022.1:n.*287C>T | |
| NM_001029852.2:c.*287C>T (PDE8B) | NP_001025023.1:n.*287C>T | |
| NM_001029853.2:c.*287C>T (PDE8B) | NP_001025024.1:n.*287C>T | |
| NM_001029854.2:c.*287C>T (PDE8B) | NP_001025025.1:n.*287C>T | |
| NM_003719.3:c.*287C>T (PDE8B) | NP_003710.1:n.*287C>T | |
| XM_005248621.3:c.*287C>T (PDE8B) | XP_005248678.1:n.*287C>T | |
| XM_005248623.3:c.*287C>T (PDE8B) | XP_005248680.1:n.*287C>T | |
| XM_005248624.3:c.*287C>T (PDE8B) | XP_005248681.1:n.*287C>T | |
| XM_006714725.2:c.*287C>T (PDE8B) | XP_006714788.1:n.*287C>T | |
| XM_006714726.2:c.*287C>T (PDE8B) | XP_006714789.1:n.*287C>T | |
| XM_011543699.1:c.*373C>T (PDE8B) | XP_011542001.1:n.*373C>T | |
| XM_011543700.1:c.*287C>T (PDE8B) | XP_011542002.1:n.*287C>T | |
| XM_011543701.1:c.*287C>T (PDE8B) | XP_011542003.1:n.*287C>T | |
| XM_011543702.1:c.*287C>T (PDE8B) | XP_011542004.1:n.*287C>T | |
| XM_011543703.1:c.*287C>T (PDE8B) | XP_011542005.1:n.*287C>T | |
| XM_011543704.1:c.*287C>T (PDE8B) | XP_011542006.1:n.*287C>T | |
| NM_001349748.1:c.*287C>T (PDE8B) | NP_001336677.1:n.*287C>T | |
| NM_001349749.1:c.*287C>T (PDE8B) | NP_001336678.1:n.*287C>T | |
| NM_001349750.1:c.*287C>T (PDE8B) | NP_001336679.1:n.*287C>T | |
| NM_001349751.1:c.*373C>T (PDE8B) | NP_001336680.1:n.*373C>T | |
| NM_001349752.1:c.*287C>T (PDE8B) | NP_001336681.1:n.*287C>T | |
| NM_001349753.1:c.*287C>T (PDE8B) | NP_001336682.1:n.*287C>T | |
| XM_005248623.4:c.*287C>T (PDE8B) | XP_005248680.1:n.*287C>T | |
| XM_006714726.3:c.*287C>T (PDE8B) | XP_006714789.1:n.*287C>T | |
| XM_011543699.3:c.*373C>T (PDE8B) | XP_011542001.1:n.*373C>T | |
| XM_011543700.3:c.*287C>T (PDE8B) | XP_011542002.1:n.*287C>T | |
| XM_011543704.2:c.*287C>T (PDE8B) | XP_011542006.1:n.*287C>T | |
| XM_017010005.2:c.*287C>T (PDE8B) | XP_016865494.1:n.*287C>T | |
| XM_017010007.2:c.*373C>T (PDE8B) | XP_016865496.1:n.*373C>T | |
| XM_017010008.2:c.*287C>T (PDE8B) | XP_016865497.1:n.*287C>T | |
| XM_024446253.1:c.*287C>T (PDE8B) | XP_024302021.1:n.*287C>T | |
| XM_024446254.1:c.*287C>T (PDE8B) | XP_024302022.1:n.*287C>T | |
| XR_001742140.1:n.2103G>A (WDR41) | ||
| NM_001029851.4:c.*287C>T (PDE8B) | NP_001025022.1:n.*287C>T | |
| NM_001029852.4:c.*287C>T (PDE8B) | NP_001025023.1:n.*287C>T | |
| NM_001029853.4:c.*287C>T (PDE8B) | NP_001025024.1:n.*287C>T | |
| NM_001029854.4:c.*287C>T (PDE8B) | NP_001025025.1:n.*287C>T | |
| NM_001349748.3:c.*287C>T (PDE8B) | NP_001336677.1:n.*287C>T | |
| NM_001349749.3:c.*287C>T (PDE8B) | NP_001336678.1:n.*287C>T | |
| NM_001349750.3:c.*287C>T (PDE8B) | NP_001336679.1:n.*287C>T | |
| NM_001349751.3:c.*373C>T (PDE8B) | NP_001336680.1:n.*373C>T | |
| NM_001349752.3:c.*287C>T (PDE8B) | NP_001336681.1:n.*287C>T | |
| NM_001349753.2:c.*287C>T (PDE8B) | NP_001336682.1:n.*287C>T | |
| NM_001376062.1:c.*287C>T (PDE8B) | NP_001362991.1:n.*287C>T | |
| NM_001376063.1:c.*287C>T (PDE8B) | NP_001362992.1:n.*287C>T | |
| NM_001376064.1:c.*287C>T (PDE8B) | NP_001362993.1:n.*287C>T | |
| NM_001376065.1:c.*287C>T (PDE8B) | NP_001362994.1:n.*287C>T | |
| NM_001376066.1:c.*287C>T (PDE8B) | NP_001362995.1:n.*287C>T | |
| NM_001376067.1:c.*287C>T (PDE8B) | NP_001362996.1:n.*287C>T | |
| NM_001376068.1:c.*287C>T (PDE8B) | NP_001362997.1:n.*287C>T | |
| NM_001376069.1:c.*287C>T (PDE8B) | NP_001362998.1:n.*287C>T | |
| NM_001376070.1:c.*287C>T (PDE8B) | NP_001362999.1:n.*287C>T | |
| NM_001376071.1:c.*287C>T (PDE8B) | NP_001363000.1:n.*287C>T | |
| NM_001376072.1:c.*373C>T (PDE8B) | NP_001363001.1:n.*373C>T | |
| NM_001376073.1:c.*287C>T (PDE8B) | NP_001363002.1:n.*287C>T | |
| NM_001376074.1:c.*287C>T (PDE8B) | NP_001363003.1:n.*287C>T | |
| NM_001376075.1:c.*287C>T (PDE8B) | NP_001363004.1:n.*287C>T | |
| NM_003719.5:c.*287C>T (PDE8B) MANE Select | NP_003710.1:n.*287C>T |