ClinVar Miner

List of variants in gene CD79A reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_001783.4(CD79A):c.419C>A (p.Thr140Asn) rs148797987 0.00126
NM_001783.4(CD79A):c.371G>A (p.Arg124His) rs144367487 0.00088
NM_001783.4(CD79A):c.224C>T (p.Thr75Met) rs199967393 0.00029
NM_001783.4(CD79A):c.269C>T (p.Thr90Met) rs137953079 0.00028
NM_001783.4(CD79A):c.134G>C (p.Ser45Thr) rs199603062 0.00024
NM_001783.4(CD79A):c.341C>T (p.Ser114Leu) rs145895409 0.00024
NM_001783.4(CD79A):c.467C>T (p.Ala156Val) rs202097187 0.00014
NM_001783.4(CD79A):c.593T>C (p.Met198Thr) rs532288711 0.00012
NM_001783.4(CD79A):c.179A>G (p.Asn60Ser) rs370313642 0.00011
NM_001783.4(CD79A):c.370C>T (p.Arg124Cys) rs144006380 0.00011
NM_001783.4(CD79A):c.203G>A (p.Arg68His) rs782507150 0.00006
NM_001783.4(CD79A):c.395C>T (p.Pro132Leu) rs201206281 0.00006
NM_001783.4(CD79A):c.466G>A (p.Ala156Thr) rs782150073 0.00006
NM_001783.4(CD79A):c.263A>G (p.Asn88Ser) rs570673845 0.00005
NM_001783.4(CD79A):c.164C>T (p.Pro55Leu) rs764758292 0.00004
NM_001783.4(CD79A):c.309A>G (p.Ile103Met) rs113019286 0.00004
NM_001783.4(CD79A):c.313G>A (p.Val105Met) rs782661874 0.00004
NM_001783.4(CD79A):c.320G>A (p.Arg107Gln) rs143511203 0.00004
NM_001783.4(CD79A):c.583G>A (p.Asp195Asn) rs782658262 0.00004
NM_001783.4(CD79A):c.224C>A (p.Thr75Lys) rs199967393 0.00003
NM_001783.4(CD79A):c.469G>A (p.Val157Met) rs1320852597 0.00003
NM_001783.4(CD79A):c.259C>T (p.Pro87Ser) rs1383830014 0.00002
NM_001783.4(CD79A):c.535G>A (p.Gly179Arg) rs782714583 0.00002
NM_001783.4(CD79A):c.653T>A (p.Ile218Lys) rs781969358 0.00002
NM_001783.4(CD79A):c.184G>A (p.Ala62Thr) rs782467376 0.00001
NM_001783.4(CD79A):c.258C>A (p.Asp86Glu) rs587778166 0.00001
NM_001783.4(CD79A):c.358G>A (p.Gly120Ser) rs782282654 0.00001
NM_001783.4(CD79A):c.373G>A (p.Val125Met) rs548487112 0.00001
NM_001783.4(CD79A):c.377G>A (p.Arg126His) rs782709381 0.00001
NM_001783.4(CD79A):c.452T>C (p.Ile151Thr) rs1221821073 0.00001
NM_001783.4(CD79A):c.650A>T (p.Asn217Ile) rs1027659418 0.00001
NM_001783.4(CD79A):c.677C>T (p.Pro226Leu) rs1555844167 0.00001
NM_001783.4(CD79A):c.80-3C>T rs781874528 0.00001
NM_001783.4(CD79A):c.8G>C (p.Gly3Ala) rs782206373 0.00001
NM_001783.4(CD79A):c.128T>A (p.Met43Lys) rs782421590
NM_001783.4(CD79A):c.137T>C (p.Leu46Pro) rs2074204859
NM_001783.4(CD79A):c.182A>T (p.Asn61Ile) rs2074205317
NM_001783.4(CD79A):c.188A>G (p.Asn63Ser) rs151224661
NM_001783.4(CD79A):c.188A>T (p.Asn63Ile)
NM_001783.4(CD79A):c.190G>A (p.Val64Ile)
NM_001783.4(CD79A):c.202C>T (p.Arg68Cys) rs782657641
NM_001783.4(CD79A):c.242T>C (p.Leu81Ser)
NM_001783.4(CD79A):c.253G>A (p.Glu85Lys)
NM_001783.4(CD79A):c.310T>C (p.Tyr104His) rs2123304241
NM_001783.4(CD79A):c.335A>G (p.Asn112Ser)
NM_001783.4(CD79A):c.338A>G (p.Glu113Gly)
NM_001783.4(CD79A):c.374T>G (p.Val125Gly) rs2123304410
NM_001783.4(CD79A):c.379+3G>A
NM_001783.4(CD79A):c.394C>A (p.Pro132Thr)
NM_001783.4(CD79A):c.416G>A (p.Gly139Asp)
NM_001783.4(CD79A):c.419C>T (p.Thr140Ile) rs148797987
NM_001783.4(CD79A):c.428G>A (p.Arg143Gln)
NM_001783.4(CD79A):c.442G>A (p.Glu148Lys) rs2074209426
NM_001783.4(CD79A):c.463_464delinsCT (p.Cys155Leu)
NM_001783.4(CD79A):c.466_467delinsTT (p.Ala156Leu)
NM_001783.4(CD79A):c.493T>C (p.Phe165Leu)
NM_001783.4(CD79A):c.498+6C>A
NM_001783.4(CD79A):c.498G>C (p.Arg166Ser) rs2123305225
NM_001783.4(CD79A):c.502C>G (p.Arg168Gly) rs1555844064
NM_001783.4(CD79A):c.503G>A (p.Arg168Gln)
NM_001783.4(CD79A):c.514G>A (p.Glu172Lys)
NM_001783.4(CD79A):c.523G>A (p.Gly175Arg) rs1016097078
NM_001783.4(CD79A):c.576C>A (p.Asn192Lys)
NM_001783.4(CD79A):c.610C>G (p.Arg204Gly) rs782417731
NM_001783.4(CD79A):c.611G>A (p.Arg204Gln) rs782624281
NM_001783.4(CD79A):c.643A>G (p.Ser215Gly) rs550589218
NM_001783.4(CD79A):c.64T>A (p.Ser22Thr) rs1600629998
NM_001783.4(CD79A):c.664C>T (p.Gln222Ter)
NM_001783.4(CD79A):c.677C>A (p.Pro226Gln) rs1555844167
NM_001783.4(CD79A):c.79+6T>C
NM_001783.4(CD79A):c.80G>T (p.Gly27Val) rs2074204427

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