ClinVar Miner

List of variants in gene combination CD79B, GH-LCR 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: 11
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HGVS dbSNP
NM_001039933.3(CD79B):c.211G>A (p.Ala71Thr)
NM_001039933.3(CD79B):c.221A>C (p.Asn74Thr) rs200126941
NM_001039933.3(CD79B):c.253G>A (p.Glu85Lys) rs373082402
NM_001039933.3(CD79B):c.289A>G (p.Met97Val)
NM_001039933.3(CD79B):c.326C>T (p.Thr109Ile) rs763307022
NM_001039933.3(CD79B):c.341G>A (p.Arg114Gln)
NM_001039933.3(CD79B):c.365_369delinsGC (p.Phe122del)
NM_001039933.3(CD79B):c.417A>G (p.Thr139=) rs1567810051
NM_001039933.3(CD79B):c.425G>A (p.Arg142Gln) rs777737578
NM_001039933.3(CD79B):c.595-6C>G rs372665115
NM_001039933.3(CD79B):c.638C>T (p.Thr213Met)

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