List of variants in gene PROM1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006017.3(PROM1):c.1497C>T (p.Ile499=)	rs113895168	0.00322
NM_006017.3(PROM1):c.1977C>T (p.Asn659=)	rs149028760	0.00222
NM_006017.3(PROM1):c.1345G>A (p.Val449Met)	rs200620291	0.00152
NM_006017.3(PROM1):c.1928C>G (p.Ala643Gly)	rs62617075	0.00065
NM_006017.3(PROM1):c.2284A>G (p.Ser762Gly)	rs202029748	0.00058
NM_006017.3(PROM1):c.2253A>G (p.Glu751=)	rs368580524	0.00044
NM_006017.3(PROM1):c.1856A>G (p.Gln619Arg)	rs905919709	0.00001
NM_006017.3(PROM1):c.102T>C (p.Tyr34=)
NM_006017.3(PROM1):c.1683-8T>A	rs1721723050
NM_006017.3(PROM1):c.906C>T (p.Leu302=)	rs1578055879

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