ClinVar Miner

List of variants in gene CDON reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_001378964.1(CDON):c.2462G>A (p.Arg821His) rs146660717 0.00102
NM_001378964.1(CDON):c.1263T>C (p.Phe421=) rs191544852 0.00056
NM_001378964.1(CDON):c.1855G>C (p.Asp619His) rs141081456 0.00056
NM_001378964.1(CDON):c.1041C>T (p.His347=) rs201963480 0.00031
NM_001378964.1(CDON):c.1426G>A (p.Val476Ile) rs142603462 0.00030
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.3190A>G (p.Ser1064Gly) rs143111106 0.00019
NM_001378964.1(CDON):c.2432G>A (p.Arg811His) rs200008378 0.00016
NM_001378964.1(CDON):c.1302G>A (p.Pro434=) rs375157917 0.00014
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.3191G>A (p.Ser1064Asn) rs113558382 0.00009
NM_001378964.1(CDON):c.2268C>T (p.Val756=) rs756370097 0.00008
NM_001378964.1(CDON):c.76+16G>A rs769492160 0.00008
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.2836T>C (p.Leu946=) rs144054280 0.00006
NM_001378964.1(CDON):c.309C>T (p.Ile103=) rs369898224 0.00006
NM_001378964.1(CDON):c.349+3G>A rs776591632 0.00006
NM_001378964.1(CDON):c.1906A>G (p.Ser636Gly) rs758389908 0.00005
NM_001378964.1(CDON):c.1254C>T (p.Asp418=) rs144423020 0.00004
NM_001378964.1(CDON):c.2567A>G (p.Asn856Ser) rs768131084 0.00004
NM_001378964.1(CDON):c.3213C>T (p.Ser1071=) rs768648215 0.00004
NM_001378964.1(CDON):c.3576C>T (p.Asp1192=) rs200023158 0.00004
NM_001378964.1(CDON):c.3631+10G>A rs771408542 0.00004
NM_001378964.1(CDON):c.846G>A (p.Pro282=) rs780286345 0.00004
NM_001378964.1(CDON):c.999C>T (p.Cys333=) rs201493965 0.00004
NM_001378964.1(CDON):c.2763C>T (p.Cys921=) rs146413034 0.00003
NM_001378964.1(CDON):c.1233A>C (p.Pro411=) rs183629033 0.00002
NM_001378964.1(CDON):c.2159-14G>A rs752818698 0.00002
NM_001378964.1(CDON):c.2205A>G (p.Thr735=) rs1264067811 0.00002
NM_001378964.1(CDON):c.108C>T (p.Leu36=) rs1358831879 0.00001
NM_001378964.1(CDON):c.1198+15C>T rs371220251 0.00001
NM_001378964.1(CDON):c.1364C>T (p.Ser455Leu) rs187095965 0.00001
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.1002C>T (p.Asp334=)
NM_001378964.1(CDON):c.1199-8T>C rs1591382720
NM_001378964.1(CDON):c.1227G>A (p.Thr409=)
NM_001378964.1(CDON):c.1347A>G (p.Pro449=) rs1464883955
NM_001378964.1(CDON):c.1365G>A (p.Ser455=)
NM_001378964.1(CDON):c.1389A>C (p.Ser463=)
NM_001378964.1(CDON):c.1485G>A (p.Ala495=) rs371467859
NM_001378964.1(CDON):c.1485G>C (p.Ala495=)
NM_001378964.1(CDON):c.1553-16C>G
NM_001378964.1(CDON):c.1553-8C>G rs774456157
NM_001378964.1(CDON):c.1553-9T>C
NM_001378964.1(CDON):c.1746A>T (p.Ile582=) rs2134599747
NM_001378964.1(CDON):c.2001C>T (p.Ala667=)
NM_001378964.1(CDON):c.2036C>A (p.Ala679Glu)
NM_001378964.1(CDON):c.2091C>G (p.Pro697=)
NM_001378964.1(CDON):c.2091C>T (p.Pro697=)
NM_001378964.1(CDON):c.2159-6G>C rs1196675375
NM_001378964.1(CDON):c.2159-9C>T
NM_001378964.1(CDON):c.2307A>G (p.Ala769=) rs2134543477
NM_001378964.1(CDON):c.2544+7A>G rs2134523703
NM_001378964.1(CDON):c.2631C>T (p.Tyr877=)
NM_001378964.1(CDON):c.2774-4C>T
NM_001378964.1(CDON):c.2995+16A>G
NM_001378964.1(CDON):c.3277-15C>T
NM_001378964.1(CDON):c.3477A>G (p.Val1159=) rs1591539667
NM_001378964.1(CDON):c.349+14T>C
NM_001378964.1(CDON):c.349+17C>T
NM_001378964.1(CDON):c.3762G>T (p.Pro1254=)
NM_001378964.1(CDON):c.497-20G>T
NM_001378964.1(CDON):c.531G>A (p.Gln177=)
NM_001378964.1(CDON):c.640+10T>C
NM_001378964.1(CDON):c.641-19A>G
NM_001378964.1(CDON):c.711C>T (p.Ser237=)
NM_001378964.1(CDON):c.76+14del rs746012079
NM_001378964.1(CDON):c.77-16G>A
NM_001378964.1(CDON):c.77-4G>C
NM_001378964.1(CDON):c.774C>T (p.Asp258=)
NM_001378964.1(CDON):c.789A>C (p.Ala263=) rs1947495706
NM_001378964.1(CDON):c.792A>G (p.Pro264=) rs1591390629
NM_001378964.1(CDON):c.891A>G (p.Gly297=)
NM_001378964.1(CDON):c.952C>T (p.Leu318=) rs1591388586

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