ClinVar Miner

List of variants in gene MAP3K8 reported as benign for not provided

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_005204.4(MAP3K8):c.336+261T>C rs303447 0.74283
NM_005204.4(MAP3K8):c.505-129A>G rs303428 0.50640
NM_005204.4(MAP3K8):c.767-188G>A rs303426 0.49474
NM_005204.4(MAP3K8):c.336+47A>G rs2907 0.46673
NM_005204.4(MAP3K8):c.234T>C (p.Tyr78=) rs1042058 0.45386
NM_005204.4(MAP3K8):c.1274-44G>T rs8177033 0.03948
NM_005204.4(MAP3K8):c.874-189C>T rs8177025 0.03366
NM_005204.4(MAP3K8):c.159T>C (p.Ser53=) rs77186746 0.01884
NM_005204.4(MAP3K8):c.915A>T (p.Ser305=) rs8177062 0.00751
NM_005204.4(MAP3K8):c.948G>A (p.Thr316=) rs114464695 0.00394
NM_005204.4(MAP3K8):c.1026+16C>T rs73247429 0.00198
NM_005204.4(MAP3K8):c.1056C>T (p.Asp352=) rs137991584 0.00157
NM_005204.4(MAP3K8):c.1269T>C (p.Ile423=) rs139333853 0.00087
NM_005204.4(MAP3K8):c.1273+12C>T rs200798807 0.00082
NM_005204.4(MAP3K8):c.1280C>T (p.Ser427Leu) rs143676953 0.00080
NM_005204.4(MAP3K8):c.222A>C (p.Ser74=) rs55962705 0.00068
NM_005204.4(MAP3K8):c.336+19A>T rs144299935 0.00024
NM_005204.4(MAP3K8):c.1026+40_1026+41dup rs9299646
NM_005204.4(MAP3K8):c.1026+41dup rs9299646
NM_005204.4(MAP3K8):c.1273+170dup rs758260441
NM_005204.4(MAP3K8):c.1273+68T>C rs8177029
NM_005204.4(MAP3K8):c.1344C>T (p.Leu448=) rs8177034
NM_005204.4(MAP3K8):c.336+286C>T rs303446

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