ClinVar Miner

List of variants in gene CDON reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_001378964.1(CDON):c.3662T>A (p.Ile1221Asn) rs684535 0.74435
NM_001378964.1(CDON):c.223G>A (p.Val75Ile) rs3740912 0.64193
NM_001378964.1(CDON):c.3294G>A (p.Thr1098=) rs3740904 0.37090
NM_001378964.1(CDON):c.2037G>A (p.Ala679=) rs516664 0.34680
NM_001378964.1(CDON):c.3165T>C (p.Asn1055=) rs564214 0.32369
NM_001378964.1(CDON):c.3039C>T (p.Asn1013=) rs684805 0.31531
NM_001378964.1(CDON):c.2545-42A>G rs2155355 0.31320
NM_001378964.1(CDON):c.3549C>T (p.Val1183=) rs2276061 0.25099
NM_001378964.1(CDON):c.76+21G>A rs1939890 0.17218
NM_001378964.1(CDON):c.2057C>T (p.Ala686Val) rs12274923 0.16080
NM_001378964.1(CDON):c.496+45C>T rs11826465 0.10354
NM_001378964.1(CDON):c.641-41G>A rs7119527 0.10343
NM_001378964.1(CDON):c.350-13T>C rs3740910 0.10340
NM_001378964.1(CDON):c.484G>A (p.Glu162Lys) rs3740909 0.10334
NM_001378964.1(CDON):c.640+12G>A rs4426144 0.10328
NM_001378964.1(CDON):c.496+50T>C rs75029148 0.07693
NM_001378964.1(CDON):c.2996-48G>T rs3824922 0.03691
NM_001378964.1(CDON):c.330T>C (p.Pro110=) rs35131477 0.03518
NM_001378964.1(CDON):c.3526G>A (p.Val1176Ile) rs78304400 0.02598
NM_001378964.1(CDON):c.2623A>G (p.Ser875Gly) rs115533243 0.02079
NM_001378964.1(CDON):c.1671G>A (p.Lys557=) rs35884952 0.01761
NM_001378964.1(CDON):c.1296G>A (p.Pro432=) rs11220313 0.01713
NM_001378964.1(CDON):c.1051C>G (p.Pro351Ala) rs35665264 0.01595
NM_001378964.1(CDON):c.9G>A (p.Pro3=) rs113593771 0.00955
NM_001378964.1(CDON):c.3559C>T (p.Arg1187Cys) rs150174788 0.00647
NM_001378964.1(CDON):c.2051C>G (p.Thr684Ser) rs145983470 0.00624
NM_001378964.1(CDON):c.3588C>T (p.Asp1196=) rs140895899 0.00553
NM_001378964.1(CDON):c.2279G>A (p.Arg760Gln) rs150587299 0.00139
NM_001378964.1(CDON):c.2462G>A (p.Arg821His) rs146660717 0.00102
NM_001378964.1(CDON):c.726G>A (p.Glu242=) rs142667570 0.00040
NM_001378964.1(CDON):c.3631+9G>A rs189386496 0.00039
NM_001378964.1(CDON):c.1041C>T (p.His347=) rs201963480 0.00031
NM_001378964.1(CDON):c.1089C>T (p.Asn363=) rs141744145 0.00028
NM_001378964.1(CDON):c.3706G>A (p.Glu1236Lys) rs373765094 0.00021
NM_001378964.1(CDON):c.1025A>G (p.Asn342Ser) rs140975280 0.00020
NM_001378964.1(CDON):c.2432G>A (p.Arg811His) rs200008378 0.00016
NM_001378964.1(CDON):c.3099C>T (p.His1033=) rs202230295 0.00014
NM_001378964.1(CDON):c.3120C>T (p.Gly1040=) rs200405251 0.00014
NM_001378964.1(CDON):c.3459T>C (p.Ser1153=) rs186048531 0.00010
NM_001378964.1(CDON):c.1414C>G (p.Pro472Ala) rs750020763 0.00009
NM_001378964.1(CDON):c.3191G>A (p.Ser1064Asn) rs113558382 0.00009
NM_001378964.1(CDON):c.2859G>T (p.Gly953=) rs139149075 0.00004
NM_001378964.1(CDON):c.2159-8G>A rs759480175 0.00003
NM_001378964.1(CDON):c.1553-17TC[6]
NM_001378964.1(CDON):c.1568A>G (p.Asn523Ser)
NM_001378964.1(CDON):c.1710C>T (p.Asn570=)
NM_001378964.1(CDON):c.1782C>T (p.Tyr594=)
NM_001378964.1(CDON):c.1824C>A (p.Ile608=)
NM_001378964.1(CDON):c.2211C>T (p.Val737=)
NM_001378964.1(CDON):c.2348G>A (p.Arg783His)
NM_001378964.1(CDON):c.2362+49C>A rs11220309
NM_001378964.1(CDON):c.2363-37GTT[3] rs138741332
NM_001378964.1(CDON):c.244C>T (p.Leu82=) rs552008016
NM_001378964.1(CDON):c.2685G>A (p.Gln895=)
NM_001378964.1(CDON):c.2996-31C>T
NM_001378964.1(CDON):c.2996-45_2996-42del rs113796011
NM_001378964.1(CDON):c.3027A>T (p.Gly1009=)
NM_001378964.1(CDON):c.3185A>C (p.Asn1062Thr)
NM_001378964.1(CDON):c.3203G>A (p.Gly1068Glu)
NM_001378964.1(CDON):c.3214G>A (p.Gly1072Arg)
NM_001378964.1(CDON):c.3390C>G (p.Ser1130Arg)
NM_001378964.1(CDON):c.349+39dup rs3832751
NM_001378964.1(CDON):c.3505G>A (p.Gly1169Ser)
NM_001378964.1(CDON):c.3560G>A (p.Arg1187His)
NM_001378964.1(CDON):c.403dup (p.Ser135fs)
NM_001378964.1(CDON):c.531G>A (p.Gln177=)
NM_001378964.1(CDON):c.985G>A (p.Val329Ile)

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