ClinVar Miner

List of variants in gene CDAN1 reported as uncertain significance for anemia (disease)

Included ClinVar conditions (263):
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Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NM_138477.4(CDAN1):c.*223G>C rs568387944
NM_138477.4(CDAN1):c.*249_*252GTTT[1] rs767935615
NM_138477.4(CDAN1):c.*349A>G rs886051156
NM_138477.4(CDAN1):c.*58G>A rs567117839
NM_138477.4(CDAN1):c.*600A>G rs886051155
NM_138477.4(CDAN1):c.*722G>A rs528323093
NM_138477.4(CDAN1):c.*775_*778AACA[1] rs531320636
NM_138477.4(CDAN1):c.*788G>T rs886051154
NM_138477.4(CDAN1):c.*827A>G rs573659922
NM_138477.4(CDAN1):c.-14G>A rs190314153
NM_138477.4(CDAN1):c.-4C>G rs776319103
NM_138477.4(CDAN1):c.1058-11T>G rs372671684
NM_138477.4(CDAN1):c.1322C>T (p.Ala441Val) rs886051158
NM_138477.4(CDAN1):c.1489_1494AGCCAC[3] (p.497_498SH[3]) rs778227051
NM_138477.4(CDAN1):c.1524A>G (p.Gln508=) rs147500837
NM_138477.4(CDAN1):c.1740-10T>A rs886051157
NM_138477.4(CDAN1):c.1766A>G (p.Asp589Gly) rs148074362
NM_138477.4(CDAN1):c.1839G>A (p.Gly613=) rs148994527
NM_138477.4(CDAN1):c.1967C>G (p.Thr656Ser) rs139202766
NM_138477.4(CDAN1):c.2007+11G>A rs758515470
NM_138477.4(CDAN1):c.2008-8C>T rs201733620
NM_138477.4(CDAN1):c.2016G>A (p.Pro672=) rs371799686
NM_138477.4(CDAN1):c.2059C>T (p.Arg687Cys) rs181448047
NM_138477.4(CDAN1):c.2197A>C (p.Ser733Arg) rs150491625
NM_138477.4(CDAN1):c.2361G>A (p.Ala787=) rs377342875
NM_138477.4(CDAN1):c.237G>C (p.Ser79=) rs180857061
NM_138477.4(CDAN1):c.2406C>T (p.Ile802=) rs145050561
NM_138477.4(CDAN1):c.2428G>C (p.Ala810Pro) rs747975571
NM_138477.4(CDAN1):c.2463G>A (p.Gly821=) rs139809959
NM_138477.4(CDAN1):c.2516C>T (p.Pro839Leu) rs772668700
NM_138477.4(CDAN1):c.2539C>T (p.Gln847Ter) rs144546360
NM_138477.4(CDAN1):c.255G>A (p.Arg85=) rs886051159
NM_138477.4(CDAN1):c.256C>T (p.Pro86Ser) rs543791953
NM_138477.4(CDAN1):c.2576C>T (p.Pro859Leu) rs370476233
NM_138477.4(CDAN1):c.2592_2596dup (p.Val866fs) rs1296421769
NM_138477.4(CDAN1):c.2700G>A (p.Gln900=) rs61745640
NM_138477.4(CDAN1):c.2750T>G (p.Ile917Ser) rs529452785
NM_138477.4(CDAN1):c.2805-11T>A rs200767055
NM_138477.4(CDAN1):c.2868C>T (p.Ala956=) rs150438471
NM_138477.4(CDAN1):c.2869-5C>T rs370304543
NM_138477.4(CDAN1):c.2872C>T (p.Leu958=) rs764432820
NM_138477.4(CDAN1):c.2984G>A (p.Arg995His) rs369919247
NM_138477.4(CDAN1):c.3128A>T (p.Asp1043Val) rs80338698
NM_138477.4(CDAN1):c.3142G>A (p.Val1048Ile) rs745816995
NM_138477.4(CDAN1):c.3204+5G>A rs201125492
NM_138477.4(CDAN1):c.3384G>A (p.Pro1128=) rs141832648
NM_138477.4(CDAN1):c.3559-11A>G rs375128684
NM_138477.4(CDAN1):c.3590A>T (p.Asn1197Ile) rs771780683
NM_138477.4(CDAN1):c.57G>C (p.Val19=) rs150418267
NM_138477.4(CDAN1):c.773+14G>A rs543228844
NM_138477.4(CDAN1):c.774-3T>C rs756901380

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