List of variants in gene PCCA reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000282.4(PCCA):c.1423A>G (p.Ile475Val)	rs35719359	0.04130
NM_000282.4(PCCA):c.1651G>T (p.Val551Phe)	rs61749895	0.00606
NM_000282.4(PCCA):c.1558A>T (p.Ser520Cys)	rs112237881	0.00159
NM_000282.4(PCCA):c.828T>C (p.Gly276=)	rs143838146	0.00143
NM_000282.4(PCCA):c.2172C>T (p.Leu724=)	rs150352833	0.00096
NM_000282.4(PCCA):c.2040+11dup	rs779884567	0.00087
NM_000282.4(PCCA):c.1065+5C>T	rs201597816	0.00083
NM_000282.4(PCCA):c.1850T>C (p.Leu617Pro)	rs563417983	0.00028
NM_000282.4(PCCA):c.606A>G (p.Ala202=)	rs140082586	0.00026
NM_000282.4(PCCA):c.862A>C (p.Arg288=)	rs121964957	0.00013
NM_000282.4(PCCA):c.1590A>G (p.Ser530=)	rs2152751916
NM_000282.4(PCCA):c.1746+9T>G
NM_000282.4(PCCA):c.1846-10dup
NM_000282.4(PCCA):c.2017G>C (p.Val673Leu)	rs142646074
NM_000282.4(PCCA):c.638-12_638-9del
NM_000282.4(PCCA):c.642C>T (p.Tyr214=)
NM_000282.4(PCCA):c.648C>T (p.Val216=)

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