ClinVar Miner

List of variants in gene CNTN1 reported as uncertain significance by GeneDx

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001843.4(CNTN1):c.278T>C (p.Met93Thr) rs142755965 0.00045
NM_001843.4(CNTN1):c.643A>G (p.Ser215Gly) rs138639141 0.00015
NM_001843.4(CNTN1):c.2983G>A (p.Ala995Thr) rs143416044 0.00012
NM_001843.4(CNTN1):c.2687T>C (p.Ile896Thr) rs771657279 0.00008
NM_001843.4(CNTN1):c.2644G>A (p.Gly882Arg) rs138121813 0.00006
NM_001843.4(CNTN1):c.3031G>A (p.Gly1011Ser) rs200796487 0.00006
NM_001843.4(CNTN1):c.652A>G (p.Ile218Val) rs752293954 0.00006
NM_001843.4(CNTN1):c.2284C>G (p.Pro762Ala) rs566695601 0.00003
NM_001843.4(CNTN1):c.1051C>T (p.Pro351Ser) rs769193585 0.00002
NM_001843.4(CNTN1):c.2039G>A (p.Arg680His) rs770506056 0.00001
NM_001843.4(CNTN1):c.296T>C (p.Val99Ala) rs780404377 0.00001
NM_001843.4(CNTN1):c.1442T>C (p.Ile481Thr) rs745586631
NM_001843.4(CNTN1):c.1888A>G (p.Asn630Asp) rs1064795510
NM_001843.4(CNTN1):c.1913C>A (p.Thr638Asn) rs2120374665
NM_001843.4(CNTN1):c.2685G>T (p.Met895Ile) rs1276439439
NM_001843.4(CNTN1):c.560G>A (p.Arg187Gln) rs4408370
NM_001843.4(CNTN1):c.644G>A (p.Ser215Asn) rs1555182848
NM_001843.4(CNTN1):c.895A>G (p.Asn299Asp)

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