ClinVar Miner

List of variants studied for congenital dyserythropoietic anemia type 2 by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 57
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HGVS dbSNP
NM_006363.6(SEC23B):c.*178C>T
NM_006363.6(SEC23B):c.*278T>C
NM_006363.6(SEC23B):c.*292T>G rs886056526
NM_006363.6(SEC23B):c.*308A>G
NM_006363.6(SEC23B):c.*32T>G
NM_006363.6(SEC23B):c.*448C>T rs550932027
NM_006363.6(SEC23B):c.*493A>G rs886056527
NM_006363.6(SEC23B):c.*494T>C rs561479544
NM_006363.6(SEC23B):c.*561A>C
NM_006363.6(SEC23B):c.*657A>G rs114937628
NM_006363.6(SEC23B):c.-24C>T rs115614151
NM_006363.6(SEC23B):c.-8T>C rs766083236
NM_006363.6(SEC23B):c.1198T>C (p.Phe400Leu) rs142461689
NM_006363.6(SEC23B):c.1201C>T (p.Arg401Ter) rs1403456625
NM_006363.6(SEC23B):c.1233+9A>G rs6081189
NM_006363.6(SEC23B):c.1234-11A>G
NM_006363.6(SEC23B):c.1276G>A (p.Val426Ile) rs41309927
NM_006363.6(SEC23B):c.1298C>T (p.Pro433Leu) rs17807673
NM_006363.6(SEC23B):c.1299G>A (p.Pro433=) rs767683935
NM_006363.6(SEC23B):c.1335G>A (p.Thr445=) rs146587686
NM_006363.6(SEC23B):c.1380C>A (p.Gly460=) rs201656419
NM_006363.6(SEC23B):c.1405-7C>T rs2273525
NM_006363.6(SEC23B):c.1413C>T (p.Thr471=)
NM_006363.6(SEC23B):c.1467C>G (p.His489Gln) rs2273526
NM_006363.6(SEC23B):c.1483C>T (p.Arg495Cys) rs768018657
NM_006363.6(SEC23B):c.1484G>A (p.Arg495His) rs141588462
NM_006363.6(SEC23B):c.1489C>T (p.Arg497Cys) rs727504145
NM_006363.6(SEC23B):c.1503C>T (p.Ile501=) rs147036760
NM_006363.6(SEC23B):c.1512T>C (p.Asn504=) rs138198461
NM_006363.6(SEC23B):c.1527G>A (p.Gln509=) rs201943863
NM_006363.6(SEC23B):c.1607C>A (p.Ala536Glu)
NM_006363.6(SEC23B):c.1649G>A (p.Arg550Gln) rs111572459
NM_006363.6(SEC23B):c.1665+6T>C rs371786580
NM_006363.6(SEC23B):c.1809A>G (p.Ser603=) rs139882548
NM_006363.6(SEC23B):c.202G>A (p.Ala68Thr)
NM_006363.6(SEC23B):c.2031G>A (p.Met677Ile) rs202187007
NM_006363.6(SEC23B):c.2061G>T (p.Leu687=) rs7262532
NM_006363.6(SEC23B):c.2143A>G (p.Ser715Gly)
NM_006363.6(SEC23B):c.2150del (p.Ala717fs) rs1334741748
NM_006363.6(SEC23B):c.2227C>T (p.Pro743Ser) rs375734554
NM_006363.6(SEC23B):c.2244T>C (p.Asp748=)
NM_006363.6(SEC23B):c.2298C>T (p.Ala766=) rs77945587
NM_006363.6(SEC23B):c.236G>A (p.Arg79Gln)
NM_006363.6(SEC23B):c.301A>G (p.Ile101Val) rs754320262
NM_006363.6(SEC23B):c.325G>A (p.Glu109Lys) rs121918221
NM_006363.6(SEC23B):c.389T>C (p.Ile130Thr)
NM_006363.6(SEC23B):c.490G>T (p.Val164Leu) rs36023150
NM_006363.6(SEC23B):c.519G>A (p.Val173=) rs138314893
NM_006363.6(SEC23B):c.569G>A (p.Arg190Gln) rs201160833
NM_006363.6(SEC23B):c.689+10C>T rs200020725
NM_006363.6(SEC23B):c.708C>A (p.His236Gln)
NM_006363.6(SEC23B):c.770C>T (p.Thr257Ile) rs146917730
NM_006363.6(SEC23B):c.773A>G (p.Gln258Arg) rs534770840
NM_006363.6(SEC23B):c.791G>A (p.Arg264Gln)
NM_006363.6(SEC23B):c.816T>C (p.Ile272=) rs115177758
NM_006363.6(SEC23B):c.835-7A>G rs184484121
NM_006363.6(SEC23B):c.85C>T (p.Leu29=) rs886056525

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