ClinVar Miner

List of variants in gene CDON studied for not specified

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Gene type:
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Total variants: 31
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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.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.1741A>G (p.Ile581Val) rs141782811 0.00003
NM_001378964.1(CDON):c.2818A>C (p.Ser940Arg) rs369673018 0.00001
NM_001378964.1(CDON):c.173G>A (p.Arg58His)
NM_001378964.1(CDON):c.2362+49C>A rs11220309
NM_001378964.1(CDON):c.2363-37GTT[3] rs138741332
NM_001378964.1(CDON):c.3395C>T (p.Pro1132Leu) rs754025360
NM_001378964.1(CDON):c.349+39dup rs3832751

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