ClinVar Miner

List of variants in gene CDON reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001378964.1(CDON):c.2544+229G>A rs2298477 0.04318
NM_001378964.1(CDON):c.76+211C>T rs73021217 0.04172
NM_001378964.1(CDON):c.2158+126A>G rs117774102 0.02581
NM_001378964.1(CDON):c.1671G>A (p.Lys557=) rs35884952 0.01761
NM_001378964.1(CDON):c.1051C>G (p.Pro351Ala) rs35665264 0.01595
NM_001378964.1(CDON):c.3276+294C>T rs116904334 0.00985
NM_001378964.1(CDON):c.3276+27C>T rs80012042 0.00937
NM_001378964.1(CDON):c.1851+224T>A rs117833792 0.00717
NM_001378964.1(CDON):c.2051C>G (p.Thr684Ser) rs145983470 0.00624
NM_001378964.1(CDON):c.1199-346T>C rs143835905 0.00539
NM_001378964.1(CDON):c.2923G>A (p.Val975Ile) rs113921147 0.00303
NM_001378964.1(CDON):c.*3141A>G rs191432564 0.00257
NM_001378964.1(CDON):c.2462G>A (p.Arg821His) rs146660717 0.00102
NM_001378964.1(CDON):c.3726A>C (p.Thr1242=) rs139588649 0.00046
NM_001378964.1(CDON):c.3190A>G (p.Ser1064Gly) rs143111106 0.00019
NM_001378964.1(CDON):c.1302G>A (p.Pro434=) rs375157917 0.00014
NM_001378964.1(CDON):c.1069C>A (p.Arg357=) rs200614048 0.00006
NM_001378964.1(CDON):c.2158+7A>C rs376244204 0.00006
NM_001378964.1(CDON):c.2770A>G (p.Lys924Glu) rs747965171 0.00006
NM_001378964.1(CDON):c.2836T>C (p.Leu946=) rs144054280 0.00006
NM_001378964.1(CDON):c.1233A>C (p.Pro411=) rs183629033 0.00002
NM_001378964.1(CDON):c.3489C>T (p.Ser1163=) rs1193053529 0.00001
NM_001378964.1(CDON):c.3516G>A (p.Pro1172=) rs763035768 0.00001
NM_001378964.1(CDON):c.3771C>T (p.Val1257=) rs1298454895 0.00001
NM_001378964.1(CDON):c.897A>C (p.Val299=) rs145701554 0.00001
NM_001378964.1(CDON):c.939C>A (p.Ser313=) rs543675306 0.00001
NM_001378964.1(CDON):c.1199-8T>C rs1591382720
NM_001378964.1(CDON):c.1347A>G (p.Pro449=) rs1464883955
NM_001378964.1(CDON):c.1553-17TC[3] rs762936563
NM_001378964.1(CDON):c.1553-8C>G rs774456157
NM_001378964.1(CDON):c.1890G>C (p.Thr630=) rs142039749
NM_001378964.1(CDON):c.2159-6G>C rs1196675375
NM_001378964.1(CDON):c.225T>C (p.Val75=)
NM_001378964.1(CDON):c.3477A>G (p.Val1159=) rs1591539667
NM_001378964.1(CDON):c.349+245_349+246dup rs5795473
NM_001378964.1(CDON):c.3631+43A>T
NM_001378964.1(CDON):c.3783C>A (p.Pro1261=)
NM_001378964.1(CDON):c.76+43T>C
NM_001378964.1(CDON):c.792A>G (p.Pro264=) rs1591390629

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