ClinVar Miner

List of variants in gene combination CDK4, TSPAN31 studied for not specified

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_000075.4(CDK4):c.696G>A (p.Leu232=) rs2227953 0.00692
NM_000075.4(CDK4):c.764G>A (p.Arg255His) rs144657355 0.00037
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.779T>A (p.Val260Glu) rs200215596 0.00013
NM_000075.4(CDK4):c.834T>C (p.Phe278=) rs115576923 0.00013
NM_000075.4(CDK4):c.886C>T (p.His296Tyr) rs2227954 0.00008
NM_000075.4(CDK4):c.898G>A (p.Gly300Ser) rs879254241 0.00004
NM_000075.4(CDK4):c.905C>T (p.Pro302Leu) rs749477862 0.00004
NM_000075.4(CDK4):c.753C>G (p.Pro251=) rs757333818 0.00003
NM_000075.4(CDK4):c.661G>A (p.Asp221Asn) rs587778187 0.00002
NM_000075.4(CDK4):c.763C>T (p.Arg255Cys) rs587778188 0.00002
NM_005981.5(TSPAN31):c.*1881A>G rs188641164 0.00002
NM_000075.4(CDK4):c.645T>C (p.Cys215=) rs751861614 0.00001
NM_000075.4(CDK4):c.660C>T (p.Ala220=) rs773490152 0.00001
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_000075.4(CDK4):c.801G>A (p.Ser267=) rs201744062 0.00001
NM_000075.4(CDK4):c.841C>G (p.His281Asp) rs876659522 0.00001
NM_005981.5(TSPAN31):c.*2037dup rs757684130 0.00001
NM_000075.4(CDK4):c.639C>A (p.Leu213=) rs2140383965
NM_000075.4(CDK4):c.647G>C (p.Gly216Ala) rs1955206366
NM_000075.4(CDK4):c.651C>T (p.Asn217=) rs876659462
NM_000075.4(CDK4):c.719G>C (p.Arg240Pro) rs531817742
NM_000075.4(CDK4):c.752C>G (p.Pro251Arg) rs143670820
NM_000075.4(CDK4):c.762C>T (p.Pro254=) rs753908111
NM_000075.4(CDK4):c.767C>T (p.Pro256Leu) rs1234167326
NM_005981.5(TSPAN31):c.*1223C>G rs770044583
NM_005981.5(TSPAN31):c.*1233G>A rs2140380925
NM_005981.5(TSPAN31):c.*1849C>A
NM_005981.5(TSPAN31):c.*1853CT[1] rs3211623
NM_005981.5(TSPAN31):c.*1874C>T rs2140382516
NM_005981.5(TSPAN31):c.*2031T>C rs370609910
NM_005981.5(TSPAN31):c.*2116A>C
NM_005981.5(TSPAN31):c.*2156T>A rs1446831422
NM_005981.5(TSPAN31):c.*2217A>G rs1565805871
NM_005981.5(TSPAN31):c.*2222G>T rs536249985
NM_005981.5(TSPAN31):c.*2224G>C rs1555201136

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