List of variants in gene PCCA reported as uncertain significance for not specified

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000282.4(PCCA):c.231+15C>T	rs202049874	0.00291
NM_000282.4(PCCA):c.1558A>T (p.Ser520Cys)	rs112237881	0.00159
NM_000282.4(PCCA):c.782A>G (p.Glu261Gly)	rs1169861687	0.00004
NM_000282.4(PCCA):c.2T>C (p.Met1Thr)	rs372093520	0.00003
NM_000282.4(PCCA):c.802C>T (p.Arg268Cys)	rs774738181	0.00003
NM_000282.4(PCCA):c.223G>C (p.Ala75Pro)	rs794727479	0.00001
NM_000282.4(PCCA):c.437T>C (p.Leu146Pro)	rs774457925	0.00001
GRCh37/hg19 13q32.3(chr13:101089225-101152483)x1
NC_000013.10:g.(101077986_101101505)_(101101560_101167680)dup
NM_000282.4(PCCA):c.1160C>G (p.Ala387Gly)	rs1484267212
NM_000282.4(PCCA):c.1209+6dup	rs746645726
NM_000282.4(PCCA):c.2061T>G (p.Ile687Met)
NM_000282.4(PCCA):c.729A>T (p.Arg243Ser)
NM_000282.4(PCCA):c.878A>G (p.Gln293Arg)	rs879253805

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