ClinVar Miner

List of variants in gene CHRNG reported as uncertain significance for not provided

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_005199.5(CHRNG):c.714G>T (p.Gln238His) rs17838626 0.00274
NM_005199.5(CHRNG):c.775G>A (p.Ala259Thr) rs138125827 0.00078
NM_005199.5(CHRNG):c.928A>T (p.Thr310Ser) rs145830034 0.00077
NM_005199.5(CHRNG):c.663G>A (p.Ala221=) rs150556220 0.00068
NM_005199.5(CHRNG):c.507-12G>A rs184423691 0.00036
NM_005199.5(CHRNG):c.1012T>C (p.Ser338Pro) rs776733115 0.00008
NM_005199.5(CHRNG):c.130G>A (p.Ala44Thr) rs186589083 0.00007
NM_005199.5(CHRNG):c.913A>G (p.Ile305Val) rs142582718 0.00005
NM_005199.5(CHRNG):c.330G>A (p.Pro110=) rs149931943 0.00003
NM_005199.5(CHRNG):c.806-7T>C rs773463683 0.00001
NM_005199.5(CHRNG):c.1035+5G>C
NM_005199.5(CHRNG):c.194T>C (p.Leu65Pro)
NM_005199.5(CHRNG):c.203G>A (p.Arg68Gln)
NM_005199.5(CHRNG):c.224A>G (p.Asn75Ser)
NM_005199.5(CHRNG):c.301_309dup (p.Arg101_Pro103dup) rs863223313
NM_005199.5(CHRNG):c.323G>C (p.Trp108Ser)
NM_005199.5(CHRNG):c.734TCA[1] (p.Ile246del) rs747062636
NM_005199.5(CHRNG):c.806-12G>A
NM_005199.5(CHRNG):c.86T>A (p.Leu29Gln) rs2106219773
NM_005199.5(CHRNG):c.98T>C (p.Leu33Pro)

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