List of variants in gene PCCA reported as uncertain significance by Natera, Inc.

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: 56

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HGVS	dbSNP	gnomAD frequency
NM_000282.4(PCCA):c.1676G>T (p.Trp559Leu)	rs118169528	0.00088
NM_000282.4(PCCA):c.2040+11dup	rs779884567	0.00087
NM_000282.4(PCCA):c.1896A>G (p.Thr632=)	rs61760965	0.00071
NM_000282.4(PCCA):c.1002C>T (p.Thr334=)	rs150106872	0.00044
NM_000282.4(PCCA):c.2055A>G (p.Gln685=)	rs147568036	0.00036
NM_000282.4(PCCA):c.2037C>T (p.Asp679=)	rs146870931	0.00035
NM_000282.4(PCCA):c.660C>T (p.Ala220=)	rs145826296	0.00026
NM_000282.4(PCCA):c.2101G>C (p.Ala701Pro)	rs143096615	0.00021
NM_000282.4(PCCA):c.328G>C (p.Val110Leu)	rs150788587	0.00017
NM_000282.4(PCCA):c.1519G>A (p.Val507Met)	rs146061036	0.00010
NM_000282.4(PCCA):c.36C>T (p.Val12=)	rs375516917	0.00009
NM_000282.4(PCCA):c.490A>G (p.Ile164Val)	rs539693612	0.00008
NM_000282.4(PCCA):c.522G>A (p.Met174Ile)	rs780406346	0.00006
NM_000282.4(PCCA):c.782A>G (p.Glu261Gly)	rs1169861687	0.00004
NM_000282.4(PCCA):c.819+9A>G	rs372739944	0.00004
NM_000282.4(PCCA):c.825A>G (p.Leu275=)	rs376560248	0.00004
NM_000282.4(PCCA):c.1342A>G (p.Met448Val)	rs767060690	0.00003
NM_000282.4(PCCA):c.1929C>T (p.Ala643=)	rs772945583	0.00003
NM_000282.4(PCCA):c.1933G>A (p.Glu645Lys)	rs145428347	0.00003
NM_000282.4(PCCA):c.2T>C (p.Met1Thr)	rs372093520	0.00003
NM_000282.4(PCCA):c.803G>A (p.Arg268His)	rs368047060	0.00003
NM_000282.4(PCCA):c.1275T>G (p.His425Gln)	rs548833871	0.00002
NM_000282.4(PCCA):c.590G>C (p.Gly197Ala)	rs766245108	0.00002
NM_000282.4(PCCA):c.61C>T (p.Pro21Ser)	rs369743452	0.00002
NM_000282.4(PCCA):c.1886T>G (p.Phe629Cys)	rs1400179119	0.00001
NM_000282.4(PCCA):c.1891G>A (p.Gly631Ser)	rs796052018	0.00001
NM_000282.4(PCCA):c.202G>A (p.Val68Ile)	rs768750176	0.00001
NM_000282.4(PCCA):c.484G>A (p.Val162Ile)	rs1442819667	0.00001
NM_000282.4(PCCA):c.54G>A (p.Gly18=)	rs1373903905	0.00001
NM_000282.4(PCCA):c.688C>T (p.Arg230Cys)	rs778530330	0.00001
NM_000282.4(PCCA):c.-4A>C	rs2046021682
NM_000282.4(PCCA):c.120T>C (p.Tyr40=)	rs2047399572
NM_000282.4(PCCA):c.1214C>A (p.Pro405His)	rs200874114
NM_000282.4(PCCA):c.1285-1417T>C	rs1232004179
NM_000282.4(PCCA):c.1383G>A (p.Glu461=)	rs2066768313
NM_000282.4(PCCA):c.1651G>A (p.Val551Ile)	rs61749895
NM_000282.4(PCCA):c.1760G>C (p.Gly587Ala)	rs2079091617
NM_000282.4(PCCA):c.1817G>C (p.Ser606Thr)	rs2079095516
NM_000282.4(PCCA):c.183+4_183+7del	rs1555342581
NM_000282.4(PCCA):c.1884G>A (p.Gln628=)	rs552141237
NM_000282.4(PCCA):c.1898T>G (p.Val633Gly)	rs375617644
NM_000282.4(PCCA):c.1919C>G (p.Thr640Ser)	rs1594099709
NM_000282.4(PCCA):c.1953G>A (p.Leu651=)	rs765771203
NM_000282.4(PCCA):c.2040+9TG[3]	rs751014655
NM_000282.4(PCCA):c.2082A>T (p.Lys694Asn)	rs2087964084
NM_000282.4(PCCA):c.2113G>T (p.Gly705Cys)	rs2087968295
NM_000282.4(PCCA):c.2155G>A (p.Gly719Arg)	rs141286340
NM_000282.4(PCCA):c.2162_2163insAG (p.Asp722fs)	rs749875940
NM_000282.4(PCCA):c.287T>C (p.Val96Ala)	rs2048368792
NM_000282.4(PCCA):c.370A>G (p.Met124Val)	rs748802820
NM_000282.4(PCCA):c.415G>A (p.Val139Ile)	rs770129876
NM_000282.4(PCCA):c.551C>G (p.Ala184Gly)	rs2059068868
NM_000282.4(PCCA):c.649A>G (p.Met217Val)	rs372844772
NM_000282.4(PCCA):c.914+8T>A	rs543352333
NM_000282.4(PCCA):c.929C>T (p.Ala310Val)	rs146927771
NM_000282.4(PCCA):c.999G>A (p.Gly333=)	rs2063427075

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