ClinVar Miner

List of variants in gene PRDM8 reported as benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_020226.3(PRDM8):c.1050C>T (p.Cys350=) rs374280707
NM_020226.3(PRDM8):c.1137C>A (p.Gly379=) rs144810863
NM_020226.3(PRDM8):c.117T>C (p.Ala39=) rs369098269
NM_020226.3(PRDM8):c.1447G>T (p.Ala483Ser) rs544862921
NM_020226.3(PRDM8):c.1683C>T (p.Ser561=) rs150632206
NM_020226.3(PRDM8):c.1726C>T (p.Leu576=) rs28405693
NM_020226.3(PRDM8):c.1778_1795del (p.Ala593_Ala598del) rs755316101
NM_020226.3(PRDM8):c.1857G>T (p.Leu619=) rs140737026
NM_020226.3(PRDM8):c.722C>A (p.Pro241Gln) rs200010979
NM_020226.3(PRDM8):c.972C>T (p.Gly324=) rs528863020
NM_020226.3(PRDM8):c.987G>T (p.Leu329=) rs6831357

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