ClinVar Miner

List of variants in gene SEC23B reported as uncertain significance for Congenital dyserythropoietic anemia, type II

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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_006363.6(SEC23B):c.1198T>C (p.Phe400Leu) rs142461689 0.00084
NM_006363.6(SEC23B):c.74C>A (p.Pro25His) rs6045440 0.00050
NM_006363.6(SEC23B):c.1665+6T>C rs371786580 0.00046
NM_006363.6(SEC23B):c.1335G>A (p.Thr445=) rs146587686 0.00028
NM_006363.6(SEC23B):c.1809A>G (p.Ser603=) rs139882548 0.00017
NM_006363.6(SEC23B):c.1527G>A (p.Gln509=) rs201943863 0.00016
NM_006363.6(SEC23B):c.*494T>C rs561479544 0.00012
NM_006363.6(SEC23B):c.2031G>A (p.Met677Ile) rs202187007 0.00012
NM_006363.6(SEC23B):c.2227C>T (p.Pro743Ser) rs375734554 0.00006
NM_006363.6(SEC23B):c.2129C>T (p.Thr710Met) rs752664090 0.00002
NM_006363.6(SEC23B):c.2143A>G (p.Ser715Gly) rs777442287 0.00002
NM_006363.6(SEC23B):c.*32T>G rs879811598 0.00001
NM_006363.6(SEC23B):c.*448C>T rs550932027 0.00001
NM_006363.6(SEC23B):c.*561A>C rs778992067 0.00001
NM_006363.6(SEC23B):c.1234-11A>G rs187699090 0.00001
NM_006363.6(SEC23B):c.1299G>A (p.Pro433=) rs767683935 0.00001
NM_006363.6(SEC23B):c.1380C>A (p.Gly460=) rs201656419 0.00001
NM_006363.6(SEC23B):c.1385A>G (p.Tyr462Cys) rs780978419 0.00001
NM_006363.6(SEC23B):c.1413C>T (p.Thr471=) rs900752773 0.00001
NM_006363.6(SEC23B):c.1483C>T (p.Arg495Cys) rs768018657 0.00001
NM_006363.6(SEC23B):c.2150del (p.Ala717fs) rs1334741748 0.00001
NM_006363.6(SEC23B):c.236G>A (p.Arg79Gln) rs370537015 0.00001
NM_006363.6(SEC23B):c.301A>G (p.Ile101Val) rs754320262 0.00001
NM_006363.6(SEC23B):c.*178C>T rs2060486772
NM_006363.6(SEC23B):c.*292T>G rs886056526
NM_006363.6(SEC23B):c.*308A>G rs2060487651
NM_006363.6(SEC23B):c.*493A>G rs886056527
NM_006363.6(SEC23B):c.-14-1G>A rs967988810
NM_006363.6(SEC23B):c.-8T>C rs766083236
NM_006363.6(SEC23B):c.1142C>T (p.Thr381Ile)
NM_006363.6(SEC23B):c.1201C>T (p.Arg401Ter) rs1403456625
NM_006363.6(SEC23B):c.1512-16A>G
NM_006363.6(SEC23B):c.1607C>A (p.Ala536Glu) rs535355543
NM_006363.6(SEC23B):c.1730C>T (p.Ser577Phe)
NM_006363.6(SEC23B):c.202G>A (p.Ala68Thr) rs2059977778
NM_006363.6(SEC23B):c.2244T>C (p.Asp748=) rs748290215
NM_006363.6(SEC23B):c.708C>A (p.His236Gln) rs748683327
NM_006363.6(SEC23B):c.791G>A (p.Arg264Gln) rs148239360
NM_006363.6(SEC23B):c.85C>T (p.Leu29=) rs886056525
NM_006363.6(SEC23B):c.902G>A (p.Gly301Asp)

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