ClinVar Miner

List of variants in gene CDON reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001378964.1(CDON):c.791C>A (p.Pro264Gln) rs140542787 0.00012
NM_001378964.1(CDON):c.2624G>A (p.Ser875Asn) rs770564593 0.00007
NM_001378964.1(CDON):c.1069C>A (p.Arg357=) rs200614048 0.00006
NM_001378964.1(CDON):c.983C>T (p.Thr328Ile) rs897565171 0.00001
NM_001378964.1(CDON):c.1099A>T (p.Ile367Phe)
NM_001378964.1(CDON):c.1133A>G (p.Tyr378Cys)
NM_001378964.1(CDON):c.1135C>T (p.Gln379Ter)
NM_001378964.1(CDON):c.1136A>G (p.Gln379Arg) rs2134658599
NM_001378964.1(CDON):c.136G>T (p.Val46Leu) rs2134695051
NM_001378964.1(CDON):c.1442G>A (p.Gly481Asp)
NM_001378964.1(CDON):c.1552+1G>A
NM_001378964.1(CDON):c.1663C>T (p.Pro555Ser) rs1555124296
NM_001378964.1(CDON):c.1780T>C (p.Tyr594His)
NM_001378964.1(CDON):c.1810G>T (p.Gly604Cys)
NM_001378964.1(CDON):c.192C>G (p.Asn64Lys)
NM_001378964.1(CDON):c.2056G>T (p.Ala686Ser) rs572486967
NM_001378964.1(CDON):c.2075G>T (p.Gly692Val)
NM_001378964.1(CDON):c.2189C>T (p.Ser730Phe) rs2134544510
NM_001378964.1(CDON):c.2279G>T (p.Arg760Leu)
NM_001378964.1(CDON):c.2336_2337del (p.Ser779fs) rs2134543186
NM_001378964.1(CDON):c.2441A>G (p.Gln814Arg) rs1555120762
NM_001378964.1(CDON):c.2650+1G>T
NM_001378964.1(CDON):c.2665C>A (p.His889Asn)
NM_001378964.1(CDON):c.2839G>C (p.Gly947Arg)
NM_001378964.1(CDON):c.3004C>G (p.Pro1002Ala) rs1169452825
NM_001378964.1(CDON):c.3010_3014del (p.Gly1004fs)
NM_001378964.1(CDON):c.3125T>G (p.Leu1042Arg) rs2134443104
NM_001378964.1(CDON):c.3318_3325del (p.Leu1106_Glu1107insTer)
NM_001378964.1(CDON):c.3395C>T (p.Pro1132Leu) rs754025360
NM_001378964.1(CDON):c.3472C>T (p.Pro1158Ser)
NM_001378964.1(CDON):c.3474del (p.Val1159fs)
NM_001378964.1(CDON):c.3515C>T (p.Pro1172Leu)
NM_001378964.1(CDON):c.3554C>A (p.Thr1185Asn) rs2134338858
NM_001378964.1(CDON):c.3631+11C>T
NM_001378964.1(CDON):c.363dup (p.Gly122fs) rs2134685110
NM_001378964.1(CDON):c.442C>T (p.Pro148Ser)
NM_001378964.1(CDON):c.581A>G (p.Tyr194Cys)
NM_001378964.1(CDON):c.774C>A (p.Asp258Glu)
NM_001378964.1(CDON):c.928+1G>A
NM_001378964.1(CDON):c.976G>T (p.Gly326Cys)

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