ClinVar Miner

List of variants in gene CR2 reported as uncertain significance for agammaglobulinemia

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_001006658.2(CR2):c.1180A>C (p.Asn394His)
NM_001006658.2(CR2):c.1210C>G (p.Pro404Ala)
NM_001006658.2(CR2):c.1390C>T (p.Pro464Ser) rs41313740
NM_001006658.2(CR2):c.1597A>T (p.Ile533Phe) rs762951469
NM_001006658.2(CR2):c.1659_1660insG (p.Tyr554Valfs)
NM_001006658.2(CR2):c.1931G>A (p.Cys644Tyr) rs149972318
NM_001006658.2(CR2):c.1962A>G (p.Ile654Met)
NM_001006658.2(CR2):c.2030C>T (p.Thr677Met)
NM_001006658.2(CR2):c.2228C>T (p.Ser743Phe)
NM_001006658.2(CR2):c.2298G>A (p.Trp766Ter) rs151093663
NM_001006658.2(CR2):c.2506C>T (p.Pro836Ser) rs147263584
NM_001006658.2(CR2):c.2656G>A (p.Val886Met)
NM_001006658.2(CR2):c.2738C>T (p.Pro913Leu) rs772503117
NM_001006658.2(CR2):c.2783G>A (p.Arg928Gln)
NM_001006658.2(CR2):c.2863C>T (p.His955Tyr) rs1329384177
NM_001006658.2(CR2):c.2920C>A (p.Pro974Thr)
NM_001006658.2(CR2):c.3047C>T (p.Ser1016Leu)
NM_001006658.2(CR2):c.3100C>G (p.Pro1034Ala)
NM_001006658.2(CR2):c.3187C>T (p.Arg1063Cys) rs145499318
NM_001006658.2(CR2):c.3238C>T (p.Arg1080Ter)
NM_001006658.2(CR2):c.3251C>A (p.Ser1084Tyr) rs142273168
NM_001006658.2(CR2):c.389T>C (p.Val130Ala) rs543886209
NM_001006658.2(CR2):c.424C>T (p.Arg142Ter) rs201017642
NM_001006658.2(CR2):c.452C>T (p.Pro151Leu)
NM_001006658.2(CR2):c.52G>A (p.Val18Ile) rs892246082
NM_001006658.2(CR2):c.605A>C (p.Lys202Thr) rs893377104
NM_001006658.2(CR2):c.622C>T (p.Pro208Ser)
NM_001006658.2(CR2):c.668A>G (p.Asn223Ser)
NM_001006658.2(CR2):c.721_722delTT (p.Phe241Leufs)
NM_001006658.2(CR2):c.728A>T (p.Asp243Val)
NM_001006658.2(CR2):c.784G>T (p.Gly262Ter)
NM_001006658.2(CR2):c.7G>T (p.Ala3Ser)

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