ClinVar Miner

List of variants in gene CD79A studied for agammaglobulinemia

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_001783.3(CD79A):c.188A>G (p.Asn63Ser) rs151224661
NM_001783.3(CD79A):c.198G>A (p.Trp66Ter) rs1568801716
NM_001783.3(CD79A):c.21C>T (p.Val7=) rs782746615
NM_001783.3(CD79A):c.224C>A (p.Thr75Lys) rs199967393
NM_001783.3(CD79A):c.258C>A (p.Asp86Glu) rs587778166
NM_001783.3(CD79A):c.269C>T (p.Thr90Met) rs137953079
NM_001783.3(CD79A):c.370C>T (p.Arg124Cys) rs144006380
NM_001783.3(CD79A):c.371G>A (p.Arg124His) rs144367487
NM_001783.3(CD79A):c.419C>A (p.Thr140Asn) rs148797987
NM_001783.3(CD79A):c.419C>T (p.Thr140Ile) rs148797987
NM_001783.3(CD79A):c.452T>C (p.Ile151Thr) rs1221821073
NM_001783.3(CD79A):c.502C>G (p.Arg168Gly) rs1555844064
NM_001783.3(CD79A):c.534C>T (p.Ala178=) rs367608135
NM_001783.3(CD79A):c.593T>C (p.Met198Thr) rs532288711
NM_001783.3(CD79A):c.64T>A (p.Ser22Thr) rs1600629998
NM_001783.4(CD79A):c.134G>C (p.Ser45Thr)
NM_001783.4(CD79A):c.184G>A (p.Ala62Thr)
NM_001783.4(CD79A):c.203G>A (p.Arg68His)
NM_001783.4(CD79A):c.224C>T (p.Thr75Met)
NM_001783.4(CD79A):c.309A>G (p.Ile103Met)
NM_001783.4(CD79A):c.313G>A (p.Val105Met)
NM_001783.4(CD79A):c.336C>T (p.Asn112=) rs1600631316
NM_001783.4(CD79A):c.341C>T (p.Ser114Leu)
NM_001783.4(CD79A):c.379+1G>A rs1555843601
NM_001783.4(CD79A):c.380-2A>G rs1600631593
NM_001783.4(CD79A):c.442G>A (p.Glu148Lys)
NM_001783.4(CD79A):c.467C>T (p.Ala156Val)
NM_001783.4(CD79A):c.513C>T (p.Asn171=) rs376178856
NM_001783.4(CD79A):c.535G>A (p.Gly179Arg)
NM_001783.4(CD79A):c.583G>A (p.Asp195Asn)
NM_001783.4(CD79A):c.677C>A (p.Pro226Gln)

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