ClinVar Miner

List of variants in gene CD79B, GH-LCR studied for agammaglobulinemia

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_000626.4(CD79B):c.102G>C (p.Arg34=)
NM_000626.4(CD79B):c.208G>A (p.Ala70Thr)
NM_000626.4(CD79B):c.218A>C (p.Asn73Thr) rs200126941
NM_000626.4(CD79B):c.238C>T (p.Gln80Ter) rs267606711
NM_000626.4(CD79B):c.250G>A (p.Glu84Lys) rs373082402
NM_000626.4(CD79B):c.272T>C (p.Leu91Pro)
NM_000626.4(CD79B):c.286A>G (p.Met96Val)
NM_000626.4(CD79B):c.303C>T (p.Asn101=)
NM_000626.4(CD79B):c.312C>T (p.Leu104=) rs116625909
NM_000626.4(CD79B):c.323C>T (p.Thr108Ile) rs763307022
NM_000626.4(CD79B):c.338G>A (p.Arg113Gln)
NM_000626.4(CD79B):c.362_366delinsGC (p.Phe121del)
NM_000626.4(CD79B):c.381C>T (p.Asn127=) rs1555598971
NM_000626.4(CD79B):c.409G>A (p.Gly137Ser) rs121912424
NM_000626.4(CD79B):c.414A>G (p.Thr138=) rs1567810051
NM_000626.4(CD79B):c.422G>A (p.Arg141Gln) rs777737578
NM_000626.4(CD79B):c.431-3C>T
NM_000626.4(CD79B):c.431-4G>A
NM_000626.4(CD79B):c.47C>T (p.Ala16Val)
NM_000626.4(CD79B):c.48G>A (p.Ala16=)
NM_000626.4(CD79B):c.547A>G (p.Lys183Glu)
NM_000626.4(CD79B):c.592-6C>G rs372665115
NM_000626.4(CD79B):c.635C>T (p.Thr212Met)
NM_000626.4(CD79B):c.645A>G (p.Thr215=)
NM_000626.4(CD79B):c.67+10C>A
NM_000626.4(CD79B):c.68-9A>G rs374896622

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