List of variants in gene PRDM5 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_018699.4(PRDM5):c.1283-5C>T	rs185134294	0.00213
NM_018699.4(PRDM5):c.1633T>C (p.Tyr545His)	rs142515463	0.00030
NM_018699.4(PRDM5):c.478C>T (p.Arg160Cys)	rs748667559	0.00001
NM_018699.4(PRDM5):c.111C>G (p.Pro37=)
NM_018699.4(PRDM5):c.1197T>G (p.Ser399=)
NM_018699.4(PRDM5):c.1698G>A (p.Thr566=)	rs764095834
NM_018699.4(PRDM5):c.21G>A (p.Pro7=)
NM_018699.4(PRDM5):c.237C>T (p.Ser79=)	rs374500219

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