ClinVar Miner

List of variants in gene CDON reported as uncertain significance for Holoprosencephaly sequence

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP
NM_001243597.1(CDON):c.*2351_*2352CA[12] rs35654681
NM_001243597.1(CDON):c.*2351_*2352CA[14] rs35654681
NM_001243597.1(CDON):c.*2351_*2352CA[16] rs35654681
NM_001243597.1(CDON):c.*2351_*2352CA[17] rs35654681
NM_001243597.1(CDON):c.*2377_*2378TA[10] rs140500280
NM_001243597.1(CDON):c.*2377_*2378TA[12] rs140500280
NM_001243597.1(CDON):c.*2379_*2380CA[3] rs886047955
NM_001243597.1(CDON):c.*2379_*2380CA[6] rs886047955
NM_001243597.1(CDON):c.*2381_*2382CA[3] rs886047954
NM_001243597.1(CDON):c.*2381_*2382CA[5] rs886047954
NM_016952.4(CDON):c.*1151C>T rs780047854
NM_016952.4(CDON):c.*1211A>G rs886047973
NM_016952.4(CDON):c.*1216G>A rs757413144
NM_016952.4(CDON):c.*1310dup rs886047972
NM_016952.4(CDON):c.*1327T>G rs886047971
NM_016952.4(CDON):c.*1429C>T rs886047970
NM_016952.4(CDON):c.*1506dup rs886047969
NM_016952.4(CDON):c.*1508A>G rs886047968
NM_016952.4(CDON):c.*1517G>T rs886047967
NM_016952.4(CDON):c.*1572A>G rs367911589
NM_016952.4(CDON):c.*1589G>A rs867218141
NM_016952.4(CDON):c.*1661C>T rs192397582
NM_016952.4(CDON):c.*1736C>T rs886047966
NM_016952.4(CDON):c.*1745A>G rs886047965
NM_016952.4(CDON):c.*1800A>G rs886047964
NM_016952.4(CDON):c.*1803C>T rs886047963
NM_016952.4(CDON):c.*1816C>T rs776338493
NM_016952.4(CDON):c.*2101A>G rs886047962
NM_016952.4(CDON):c.*215C>T rs879027869
NM_016952.4(CDON):c.*2195G>A rs886047961
NM_016952.4(CDON):c.*2264C>T rs185017679
NM_016952.4(CDON):c.*2283_*2285del rs879891676
NM_016952.4(CDON):c.*2345_*2349delinsAACACACACAC rs886047960
NM_016952.4(CDON):c.*2345_*2349delinsAACACACACACAC rs886047960
NM_016952.4(CDON):c.*2373C>T rs371492744
NM_016952.4(CDON):c.*2373_*2378del rs886047957
NM_016952.4(CDON):c.*2376_*2377insCACACACACACACACATATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACACACACACATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACACACACATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACACACACATATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACACACATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACACACATATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACACATATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACACATATATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCACATATATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCATA rs371911236
NM_016952.4(CDON):c.*2376_*2377insCATATA rs371911236
NM_016952.4(CDON):c.*2377T>C rs582224
NM_016952.4(CDON):c.*2377_*2379delinsCACACACACAC rs886047956
NM_016952.4(CDON):c.*2377_*2379delinsCACACACACACACAC rs886047956
NM_016952.4(CDON):c.*2377delinsCACACACACACACAC rs886047958
NM_016952.4(CDON):c.*2377delinsCACACACACACACACAC rs886047958
NM_016952.4(CDON):c.*2378_*2379insCA rs886047955
NM_016952.4(CDON):c.*2380_*2381insCA rs886047954
NM_016952.4(CDON):c.*2380_*2381insCACA rs886047954
NM_016952.4(CDON):c.*249G>A rs886047975
NM_016952.4(CDON):c.*2580G>C rs886047952
NM_016952.4(CDON):c.*2640A>G rs886047951
NM_016952.4(CDON):c.*2698T>C rs886047950
NM_016952.4(CDON):c.*2705C>T rs549903425
NM_016952.4(CDON):c.*2769G>A rs886047949
NM_016952.4(CDON):c.*3104T>C rs886047948
NM_016952.4(CDON):c.*3133A>T rs886047947
NM_016952.4(CDON):c.*3210A>G rs886047946
NM_016952.4(CDON):c.*3481C>T rs886047945
NM_016952.4(CDON):c.*3522_*3523del rs886047944
NM_016952.4(CDON):c.*3610C>T rs886047943
NM_016952.4(CDON):c.*369G>A rs147808410
NM_016952.4(CDON):c.*3916G>A rs886047942
NM_016952.4(CDON):c.*4097A>G rs886047941
NM_016952.4(CDON):c.*601T>A rs549303080
NM_016952.4(CDON):c.*609dup rs111312273
NM_016952.4(CDON):c.*696T>C rs566390376
NM_016952.4(CDON):c.*863C>T rs886047974
NM_016952.4(CDON):c.*864G>A rs144806373
NM_016952.4(CDON):c.*871C>T rs148777681
NM_016952.4(CDON):c.-48G>A rs374433009
NM_016952.4(CDON):c.-61-15del rs886047980
NM_016952.4(CDON):c.-61-9_-61-7del rs557544550
NM_016952.4(CDON):c.1000G>C (p.Asp334His) rs571859031
NM_016952.4(CDON):c.1253A>T (p.Asp418Val) rs753627841
NM_016952.4(CDON):c.1414C>G (p.Pro472Ala) rs750020763
NM_016952.4(CDON):c.1553-17TC[3] rs762936563
NM_016952.4(CDON):c.1654A>G (p.Ser552Gly) rs886047977
NM_016952.4(CDON):c.1665G>A (p.Pro555=) rs537471531
NM_016952.4(CDON):c.1741A>G (p.Ile581Val) rs141782811
NM_016952.4(CDON):c.1826A>G (p.Asn609Ser) rs756054017
NM_016952.4(CDON):c.1847G>A (p.Arg616Gln) rs144938780
NM_016952.4(CDON):c.1855G>C (p.Asp619His) rs141081456
NM_016952.4(CDON):c.1889C>T (p.Thr630Met) rs559379897
NM_016952.4(CDON):c.1940C>T (p.Pro647Leu) rs200961603
NM_016952.4(CDON):c.1977C>T (p.Ser659=) rs563267429
NM_016952.4(CDON):c.2026+15C>T rs143813933
NM_016952.4(CDON):c.2159-14G>A rs752818698
NM_016952.4(CDON):c.2159-8G>A rs759480175
NM_016952.4(CDON):c.2239G>A (p.Gly747Arg) rs745363657
NM_016952.4(CDON):c.2429C>G (p.Ser810Cys) rs746038393
NM_016952.4(CDON):c.2462G>A (p.Arg821His) rs146660717
NM_016952.4(CDON):c.3040G>A (p.Gly1014Arg) rs371732066
NM_016952.4(CDON):c.3061A>G (p.Thr1021Ala) rs762511903
NM_016952.4(CDON):c.3190A>G (p.Ser1064Gly) rs143111106
NM_016952.4(CDON):c.3297C>T (p.Ala1099=) rs770868175
NM_016952.4(CDON):c.3312C>T (p.Asp1104=) rs886047976
NM_016952.4(CDON):c.350-9A>G rs367564964
NM_016952.4(CDON):c.3603C>A (p.Gly1201=) rs763774382
NM_016952.4(CDON):c.39T>C (p.Tyr13=) rs886047979
NM_016952.4(CDON):c.94A>G (p.Thr32Ala) rs886047978

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