ClinVar Miner

List of variants in gene CC2D2A reported as uncertain significance by GeneDx

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Total variants: 27
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HGVS dbSNP
NM_001080522.2(CC2D2A):c.1484G>A (p.Arg495His) rs373906628
NM_001080522.2(CC2D2A):c.157G>A (p.Glu53Lys) rs373080748
NM_001080522.2(CC2D2A):c.1720T>A (p.Tyr574Asn) rs768277071
NM_001080522.2(CC2D2A):c.1837G>A (p.Glu613Lys) rs201439617
NM_001080522.2(CC2D2A):c.1880G>A (p.Arg627Gln) rs752576142
NM_001080522.2(CC2D2A):c.1978G>C (p.Val660Leu) rs16892134
NM_001080522.2(CC2D2A):c.2050T>A (p.Leu684Ile) rs190698163
NM_001080522.2(CC2D2A):c.2117G>A (p.Arg706Gln) rs778205727
NM_001080522.2(CC2D2A):c.2197G>A (p.Gly733Arg) rs372259202
NM_001080522.2(CC2D2A):c.2326G>A (p.Gly776Arg) rs200764366
NM_001080522.2(CC2D2A):c.2417C>T (p.Ala806Val) rs769808709
NM_001080522.2(CC2D2A):c.2624C>T (p.Ser875Leu) rs200904521
NM_001080522.2(CC2D2A):c.286G>A (p.Ala96Thr) rs376438052
NM_001080522.2(CC2D2A):c.3076A>G (p.Lys1026Glu) rs759702917
NM_001080522.2(CC2D2A):c.3113A>T (p.Asp1038Val) rs376913682
NM_001080522.2(CC2D2A):c.3135G>A (p.Val1045=) rs371608031
NM_001080522.2(CC2D2A):c.3250T>A (p.Tyr1084Asn) rs751234041
NM_001080522.2(CC2D2A):c.3320T>G (p.Phe1107Cys) rs886041156
NM_001080522.2(CC2D2A):c.380G>A (p.Arg127Gln) rs748886997
NM_001080522.2(CC2D2A):c.3869T>C (p.Val1290Ala) rs200427832
NM_001080522.2(CC2D2A):c.3872T>C (p.Ile1291Thr) rs370492044
NM_001080522.2(CC2D2A):c.3880A>C (p.Ser1294Arg) rs1064795568
NM_001080522.2(CC2D2A):c.3883G>A (p.Gly1295Arg) rs763466980
NM_001080522.2(CC2D2A):c.3976-18C>G rs375782772
NM_001080522.2(CC2D2A):c.3985G>C (p.Ala1329Pro) rs951039594
NM_001080522.2(CC2D2A):c.4729G>A (p.Ala1577Thr) rs199695154
NM_001080522.2(CC2D2A):c.970C>T (p.Arg324Cys) rs376969878

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