List of variants in gene POU2AF3 reported as uncertain significance

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001271458.2(POU2AF3):c.341T>G (p.Phe114Cys)	rs201037042	0.00083
NM_001271458.2(POU2AF3):c.649G>A (p.Ala217Thr)	rs372744042	0.00010
NM_001271458.2(POU2AF3):c.526C>G (p.Pro176Ala)	rs1016414091	0.00007
NM_001271458.2(POU2AF3):c.719A>G (p.Tyr240Cys)	rs372121303	0.00006
NM_001271458.2(POU2AF3):c.749A>G (p.Tyr250Cys)	rs540046911	0.00005
NM_001271458.2(POU2AF3):c.523C>A (p.Pro175Thr)	rs1391190802	0.00002
NM_001271458.2(POU2AF3):c.439A>G (p.Ser147Gly)	rs376560556	0.00001
NM_001271458.2(POU2AF3):c.314A>C (p.Asn105Thr)
NM_001271458.2(POU2AF3):c.379C>A (p.Gln127Lys)	rs2496563910
NM_001271458.2(POU2AF3):c.523C>G (p.Pro175Ala)
NM_001271458.2(POU2AF3):c.527C>G (p.Pro176Arg)	rs201045815
NM_001271458.2(POU2AF3):c.548A>G (p.His183Arg)
NM_001271458.2(POU2AF3):c.562G>T (p.Ala188Ser)
NM_001271458.2(POU2AF3):c.584C>T (p.Ser195Leu)
NM_001271458.2(POU2AF3):c.614C>T (p.Ser205Leu)

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