ClinVar Miner

List of variants in gene combination CDK4, TSPAN31 reported as benign

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_005981.5(TSPAN31):c.*1781C>A rs2069506 0.25021
NM_005981.5(TSPAN31):c.*529C>T rs184712 0.22296
NM_005981.5(TSPAN31):c.*798G>C rs3472 0.03579
NM_005981.5(TSPAN31):c.*865A>C rs3473 0.03562
NM_005981.5(TSPAN31):c.*714C>T rs113625101 0.03374
NM_005981.5(TSPAN31):c.*744G>A rs112275916 0.02614
NM_005981.5(TSPAN31):c.*1777A>G rs2069507 0.02320
NM_000075.4(CDK4):c.696G>A (p.Leu232=) rs2227953 0.00692
NM_005981.5(TSPAN31):c.*1025C>T rs2069511 0.00275
NM_000075.4(CDK4):c.764G>A (p.Arg255His) rs144657355 0.00037
NM_005981.5(TSPAN31):c.*484G>A rs192347082 0.00025
NM_005981.5(TSPAN31):c.*2031T>A rs370609910 0.00016
NM_000075.4(CDK4):c.771G>A (p.Val257=) rs377612647 0.00014
NM_000075.4(CDK4):c.834T>C (p.Phe278=) rs115576923 0.00013
NM_000075.4(CDK4):c.813G>A (p.Leu271=) rs1487727732 0.00011
NM_000075.4(CDK4):c.776C>T (p.Ser259Leu) rs201617914 0.00007
NM_000075.4(CDK4):c.763C>T (p.Arg255Cys) rs587778188 0.00002
NM_000075.4(CDK4):c.777G>A (p.Ser259=) rs3211622 0.00001
NM_000075.4(CDK4):c.800C>T (p.Ser267Leu) rs1157646541 0.00001
NM_005981.5(TSPAN31):c.*1414_*1415insCTT rs2140381594
NM_005981.5(TSPAN31):c.*1418_*1420dup rs145025938
NM_005981.5(TSPAN31):c.*1853CT[1] rs3211623
NM_005981.5(TSPAN31):c.*2222G>A rs536249985

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