ClinVar Miner

List of variants in gene AXL reported by Ambry Genetics

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_021913.5(AXL):c.1597C>T (p.Arg533Trp) rs144179986 0.00012
NM_021913.5(AXL):c.2270A>G (p.Glu757Gly) rs146263330 0.00011
NM_021913.5(AXL):c.2471T>C (p.Met824Thr) rs767935771 0.00005
NM_021913.5(AXL):c.1198T>C (p.Ser400Pro) rs773508947 0.00004
NM_021913.5(AXL):c.1069C>T (p.Arg357Trp) rs143593613 0.00003
NM_021913.5(AXL):c.130A>G (p.Ile44Val) rs770570685 0.00003
NM_021913.5(AXL):c.2318A>G (p.Asp773Gly) rs773904444 0.00003
NM_021913.5(AXL):c.854C>T (p.Ser285Leu) rs201003955 0.00003
NM_021913.5(AXL):c.1096G>C (p.Gly366Arg) rs763059327 0.00002
NM_021913.5(AXL):c.80C>T (p.Pro27Leu) rs1000076660 0.00002
NM_021913.5(AXL):c.905A>T (p.His302Leu) rs778289997 0.00002
NM_021913.5(AXL):c.112G>A (p.Val38Met) rs781049505 0.00001
NM_021913.5(AXL):c.11G>A (p.Arg4Gln) rs779811231 0.00001
NM_021913.5(AXL):c.142C>T (p.Arg48Trp) rs774132867 0.00001
NM_021913.5(AXL):c.1580G>A (p.Arg527Gln) rs777326148 0.00001
NM_021913.5(AXL):c.2056G>A (p.Val686Met) rs763877877 0.00001
NM_021913.5(AXL):c.2328T>A (p.Asp776Glu) rs759441780 0.00001
NM_021913.5(AXL):c.2671G>C (p.Glu891Gln) rs376230166 0.00001
NM_021913.5(AXL):c.377T>C (p.Phe126Ser) rs969922085 0.00001
NM_021913.5(AXL):c.749G>A (p.Ser250Asn) rs780756544 0.00001
NM_021913.5(AXL):c.1021A>T (p.Ser341Cys)
NM_021913.5(AXL):c.1126A>C (p.Thr376Pro) rs2516411819
NM_021913.5(AXL):c.1142T>G (p.Met381Arg)
NM_021913.5(AXL):c.1202A>G (p.Asn401Ser)
NM_021913.5(AXL):c.1238G>A (p.Gly413Glu) rs556311078
NM_021913.5(AXL):c.1308G>T (p.Gln436His)
NM_021913.5(AXL):c.1324T>G (p.Ser442Ala)
NM_021913.5(AXL):c.143G>C (p.Arg48Pro) rs200598880
NM_021913.5(AXL):c.1451T>C (p.Val484Ala) rs1051706028
NM_021913.5(AXL):c.1465G>C (p.Val489Leu)
NM_021913.5(AXL):c.1531G>A (p.Ala511Thr)
NM_021913.5(AXL):c.1568A>T (p.Lys523Met)
NM_021913.5(AXL):c.160C>A (p.Leu54Ile) rs765631388
NM_021913.5(AXL):c.1717A>G (p.Ile573Val)
NM_021913.5(AXL):c.1829G>T (p.Arg610Leu)
NM_021913.5(AXL):c.1915G>C (p.Asp639His)
NM_021913.5(AXL):c.2096A>G (p.Asn699Ser) rs1046496875
NM_021913.5(AXL):c.2257G>A (p.Val753Met)
NM_021913.5(AXL):c.2523C>A (p.Asp841Glu)
NM_021913.5(AXL):c.2566A>T (p.Thr856Ser)
NM_021913.5(AXL):c.379G>C (p.Val127Leu) rs1236482248
NM_021913.5(AXL):c.436G>A (p.Glu146Lys)
NM_021913.5(AXL):c.452C>T (p.Ala151Val)
NM_021913.5(AXL):c.461C>A (p.Thr154Asn) rs765828639
NM_021913.5(AXL):c.637G>A (p.Val213Ile)
NM_021913.5(AXL):c.650G>A (p.Arg217His) rs776682499
NM_021913.5(AXL):c.656C>G (p.Ala219Gly)
NM_021913.5(AXL):c.686G>A (p.Arg229His)
NM_021913.5(AXL):c.731C>G (p.Ala244Gly) rs950685158
NM_021913.5(AXL):c.79C>T (p.Pro27Ser)
NM_021913.5(AXL):c.806T>G (p.Met269Arg) rs2034109267
NM_021913.5(AXL):c.874C>G (p.His292Asp) rs1160421475
NM_021913.5(AXL):c.935C>T (p.Thr312Ile)
NM_021913.5(AXL):c.992G>A (p.Gly331Glu) rs2516410660

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