ClinVar Miner

List of variants reported as uncertain significance for Chudley-McCullough syndrome

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ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_013296.5(GPSM2):c.-486G>C rs190373749 0.00426
NM_013296.5(GPSM2):c.-306C>A rs550061353 0.00412
NM_013296.5(GPSM2):c.-357C>T rs564045797 0.00409
NM_001377458.1(CLCC1):c.*2256G>A rs188296554 0.00235
NM_001377458.1(CLCC1):c.*2139A>C rs568302826 0.00218
NM_013296.5(GPSM2):c.2043G>A (p.Ser681=) rs140949805 0.00176
NM_013296.5(GPSM2):c.1739C>T (p.Ser580Leu) rs79730689 0.00145
NM_013296.5(GPSM2):c.833G>A (p.Arg278Gln) rs190381417 0.00139
NM_001377458.1(CLCC1):c.*2600A>G rs193138520 0.00113
NM_013296.5(GPSM2):c.1263+11G>A rs201878481 0.00077
NM_001377458.1(CLCC1):c.*2399T>C rs542144752 0.00071
NM_013296.5(GPSM2):c.1216C>T (p.Arg406Trp) rs141562079 0.00061
NM_013296.5(GPSM2):c.-316C>T rs535833314 0.00030
NM_013296.5(GPSM2):c.1358A>G (p.Lys453Arg) rs200378397 0.00014
NM_013296.5(GPSM2):c.683G>A (p.Arg228His) rs757559568 0.00013
NM_013296.5(GPSM2):c.-248-1G>A rs1051372133 0.00010
NM_001377458.1(CLCC1):c.*2140C>A rs548199963 0.00008
NM_013296.5(GPSM2):c.2040A>G (p.Lys680=) rs142663817 0.00008
NM_013296.5(GPSM2):c.1694G>A (p.Ser565Asn) rs199536935 0.00007
NM_013296.5(GPSM2):c.1356G>A (p.Gly452=) rs377658968 0.00006
NM_013296.5(GPSM2):c.1909C>T (p.Arg637Trp) rs189033496 0.00006
NM_013296.5(GPSM2):c.358G>A (p.Glu120Lys) rs754926445 0.00006
NM_013296.5(GPSM2):c.953+12G>A rs377727537 0.00006
NM_001377458.1(CLCC1):c.*2285A>G rs886045027 0.00004
NM_013296.5(GPSM2):c.-245T>A rs886045024 0.00004
NM_013296.5(GPSM2):c.1665G>C (p.Gln555His) rs771359771 0.00004
NM_013296.5(GPSM2):c.1208T>C (p.Leu403Ser) rs747510797 0.00003
NM_013296.5(GPSM2):c.124G>A (p.Ala42Thr) rs780911321 0.00003
NM_013296.5(GPSM2):c.1910G>A (p.Arg637Gln) rs765367400 0.00003
NM_013296.5(GPSM2):c.529G>A (p.Ala177Thr) rs397517232 0.00003
NM_013296.5(GPSM2):c.-441G>C rs886045022 0.00002
NM_013296.5(GPSM2):c.-397C>G rs749825634 0.00001
NM_013296.5(GPSM2):c.1034C>G (p.Ala345Gly) rs765450533 0.00001
NM_013296.5(GPSM2):c.1244T>C (p.Met415Thr) rs150152015 0.00001
NM_013296.5(GPSM2):c.1799T>A (p.Ile600Asn) rs779688224 0.00001
NM_013296.5(GPSM2):c.186C>T (p.Ser62=) rs199575734 0.00001
NM_013296.5(GPSM2):c.274G>A (p.Ala92Thr) rs747080388 0.00001
NM_013296.5(GPSM2):c.278G>A (p.Arg93Lys) rs757227955 0.00001
NM_013296.5(GPSM2):c.597G>A (p.Ala199=) rs745395767 0.00001
NM_001377458.1(CLCC1):c.*2133A>G rs1017420538
NM_001377458.1(CLCC1):c.*2856T>C rs1651564377
NM_013296.5(GPSM2):c.-288C>A rs1665666541
NM_013296.5(GPSM2):c.-369G>A rs886045023
NM_013296.5(GPSM2):c.-426G>A rs527368687
NM_013296.5(GPSM2):c.-453C>T rs1057445821
NM_013296.5(GPSM2):c.-469C>G rs541910644
NM_013296.5(GPSM2):c.1066G>A (p.Gly356Arg) rs61754640
NM_013296.5(GPSM2):c.1472G>C (p.Gly491Ala) rs147906282
NM_013296.5(GPSM2):c.1941_1942del (p.Arg647fs)
NM_013296.5(GPSM2):c.279-6T>C rs1648461612
NM_013296.5(GPSM2):c.478G>C (p.Gly160Arg) rs1557862489
NM_013296.5(GPSM2):c.807A>G (p.Leu269=) rs752642372

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