ClinVar Miner

List of variants in gene CCDC137 studied for not specified

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_199287.3(CCDC137):c.791C>T (p.Ala264Val) rs375426067 0.00031
NM_199287.3(CCDC137):c.367G>A (p.Gly123Arg) rs199850384 0.00027
NM_199287.3(CCDC137):c.595G>C (p.Gly199Arg) rs201200598 0.00011
NM_199287.3(CCDC137):c.803G>A (p.Arg268Gln) rs769092974 0.00005
NM_199287.3(CCDC137):c.166A>G (p.Lys56Glu) rs368297027 0.00003
NM_199287.3(CCDC137):c.116C>T (p.Pro39Leu) rs1175397389 0.00001
NM_199287.3(CCDC137):c.322G>A (p.Asp108Asn) rs1444365636 0.00001
NM_199287.3(CCDC137):c.36G>T (p.Arg12Ser) rs755573812 0.00001
NM_199287.3(CCDC137):c.467A>G (p.Glu156Gly) rs763418221 0.00001
NM_199287.3(CCDC137):c.739C>T (p.Arg247Cys) rs777978705 0.00001
NM_199287.3(CCDC137):c.782C>T (p.Ala261Val) rs1379888799 0.00001
NM_199287.3(CCDC137):c.815T>C (p.Leu272Pro) rs753561494 0.00001
NM_199287.3(CCDC137):c.177C>G (p.Asp59Glu) rs1568199699
NM_199287.3(CCDC137):c.244A>G (p.Ser82Gly)
NM_199287.3(CCDC137):c.26C>T (p.Ala9Val) rs374543963
NM_199287.3(CCDC137):c.355G>T (p.Gly119Trp) rs527515702
NM_199287.3(CCDC137):c.385A>G (p.Met129Val) rs1342472268
NM_199287.3(CCDC137):c.430G>A (p.Ala144Thr) rs2509823243
NM_199287.3(CCDC137):c.437G>A (p.Arg146Gln)
NM_199287.3(CCDC137):c.498G>A (p.Ala166=)
NM_199287.3(CCDC137):c.509G>A (p.Arg170Gln)
NM_199287.3(CCDC137):c.5C>T (p.Ala2Val)
NM_199287.3(CCDC137):c.673T>C (p.Ser225Pro)
NM_199287.3(CCDC137):c.683T>G (p.Leu228Arg) rs2509825198
NM_199287.3(CCDC137):c.703G>A (p.Gly235Ser)
NM_199287.3(CCDC137):c.704G>T (p.Gly235Val)
NM_199287.3(CCDC137):c.710T>A (p.Val237Glu)
NM_199287.3(CCDC137):c.718C>T (p.Pro240Ser)
NM_199287.3(CCDC137):c.746G>A (p.Arg249Gln)
NM_199287.3(CCDC137):c.770G>A (p.Arg257Gln)
NM_199287.3(CCDC137):c.789A>C (p.Arg263Ser)
NM_199287.3(CCDC137):c.803G>T (p.Arg268Leu)
NM_199287.3(CCDC137):c.808C>G (p.Gln270Glu)
NM_199287.3(CCDC137):c.827G>A (p.Arg276Gln)
NM_199287.3(CCDC137):c.838A>T (p.Thr280Ser)
NM_199287.3(CCDC137):c.850A>G (p.Lys284Glu) rs2509825523
NM_199287.3(CCDC137):c.856G>C (p.Glu286Gln)

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