ClinVar Miner

List of variants in gene CD79A reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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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.534C>T (p.Ala178=) rs367608135 0.00107
NM_001783.4(CD79A):c.498+12C>T rs530163712 0.00020
NM_001783.4(CD79A):c.312C>T (p.Tyr104=) rs200667174 0.00016
NM_001783.4(CD79A):c.499-17C>T rs368605906 0.00008
NM_001783.4(CD79A):c.567+12G>A rs782504307 0.00007
NM_001783.4(CD79A):c.165G>A (p.Pro55=) rs144847382 0.00006
NM_001783.4(CD79A):c.372C>T (p.Arg124=) rs377615732 0.00006
NM_001783.4(CD79A):c.79+14G>A rs782665303 0.00006
NM_001783.4(CD79A):c.204C>T (p.Arg68=) rs150297110 0.00005
NM_001783.4(CD79A):c.513C>T (p.Asn171=) rs376178856 0.00005
NM_001783.4(CD79A):c.183C>T (p.Asn61=) rs781792305 0.00004
NM_001783.4(CD79A):c.225G>A (p.Thr75=) rs1487166711 0.00004
NM_001783.4(CD79A):c.301G>A (p.Gly101Arg) rs117078414 0.00004
NM_001783.4(CD79A):c.61C>T (p.Leu21=) rs1044944143 0.00004
NM_001783.4(CD79A):c.678G>A (p.Pro226=) rs782316113 0.00003
NM_001783.4(CD79A):c.147C>T (p.Asp49=) rs782302503 0.00002
NM_001783.4(CD79A):c.567+19T>G rs1215527412 0.00002
NM_001783.4(CD79A):c.270G>A (p.Thr90=) rs781875393 0.00001
NM_001783.4(CD79A):c.28G>A (p.Ala10Thr) rs371184689 0.00001
NM_001783.4(CD79A):c.30T>C (p.Ala10=) rs782716159 0.00001
NM_001783.4(CD79A):c.327G>A (p.Gln109=) rs782492918 0.00001
NM_001783.4(CD79A):c.336C>T (p.Asn112=) rs1600631316 0.00001
NM_001783.4(CD79A):c.375G>A (p.Val125=) rs1600631350 0.00001
NM_001783.4(CD79A):c.387C>T (p.Pro129=) rs1174888211 0.00001
NM_001783.4(CD79A):c.453C>T (p.Ile151=) rs1349692713 0.00001
NM_001783.4(CD79A):c.465C>T (p.Cys155=) rs537675914 0.00001
NM_001783.4(CD79A):c.483G>A (p.Thr161=) rs781984117 0.00001
NM_001783.4(CD79A):c.498+10C>A rs782338772 0.00001
NM_001783.4(CD79A):c.498+13G>A rs2074210271 0.00001
NM_001783.4(CD79A):c.54C>A (p.Leu18=) rs141033669 0.00001
NM_001783.4(CD79A):c.552T>C (p.Asp184=) rs1167492507 0.00001
NM_001783.4(CD79A):c.582C>T (p.Asp194=) rs781967496 0.00001
NM_001783.4(CD79A):c.108C>T (p.His36=)
NM_001783.4(CD79A):c.120A>C (p.Ala40=)
NM_001783.4(CD79A):c.12T>G (p.Gly4=)
NM_001783.4(CD79A):c.150C>T (p.Ala50=)
NM_001783.4(CD79A):c.189C>T (p.Asn63=)
NM_001783.4(CD79A):c.210C>A (p.Leu70=) rs2074205615
NM_001783.4(CD79A):c.21C>T (p.Val7=) rs782746615
NM_001783.4(CD79A):c.24C>T (p.Leu8=) rs2123301467
NM_001783.4(CD79A):c.309A>C (p.Ile103=) rs113019286
NM_001783.4(CD79A):c.357C>T (p.Cys119=)
NM_001783.4(CD79A):c.379+19G>T
NM_001783.4(CD79A):c.380-14C>A
NM_001783.4(CD79A):c.380-8C>T
NM_001783.4(CD79A):c.384G>A (p.Pro128=)
NM_001783.4(CD79A):c.400C>T (p.Leu134=) rs2123304949
NM_001783.4(CD79A):c.427C>A (p.Arg143=)
NM_001783.4(CD79A):c.499-15C>T rs2123307362
NM_001783.4(CD79A):c.499-18C>A
NM_001783.4(CD79A):c.499-18C>T
NM_001783.4(CD79A):c.499-8C>T
NM_001783.4(CD79A):c.519G>A (p.Lys173=)
NM_001783.4(CD79A):c.51C>A (p.Leu17=)
NM_001783.4(CD79A):c.525G>T (p.Gly175=)
NM_001783.4(CD79A):c.561T>G (p.Leu187=)
NM_001783.4(CD79A):c.567+15G>C
NM_001783.4(CD79A):c.567+20_567+21delinsAT
NM_001783.4(CD79A):c.568-16C>T
NM_001783.4(CD79A):c.568-6T>C
NM_001783.4(CD79A):c.624C>T (p.Gly208=) rs2123308093
NM_001783.4(CD79A):c.79+8G>A
NM_001783.4(CD79A):c.80-12G>A

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