ClinVar Miner

List of variants in gene CXCR4 reported as uncertain significance for leukopenia

Included ClinVar conditions (54):
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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_003467.3(CXCR4):c.157A>C (p.Ile53Leu) rs56400844 0.00045
NM_003467.3(CXCR4):c.16-14T>A rs1053292586 0.00008
NM_003467.3(CXCR4):c.506T>C (p.Ile169Thr) rs371317659 0.00008
NM_003467.3(CXCR4):c.704G>A (p.Arg235His) rs377287446 0.00006
NM_003467.3(CXCR4):c.582G>C (p.Leu194Phe) rs769772228 0.00005
NM_003467.3(CXCR4):c.748G>A (p.Ala250Thr) rs771851938 0.00005
NM_003467.3(CXCR4):c.250G>C (p.Asp84His) rs368016542 0.00003
NM_003467.3(CXCR4):c.1022C>A (p.Ser341Tyr) rs148454403 0.00001
NM_003467.3(CXCR4):c.1054A>G (p.Ser352Gly) rs750756138 0.00001
NM_003467.3(CXCR4):c.137C>G (p.Ser46Cys) rs147467366 0.00001
NM_003467.3(CXCR4):c.345C>G (p.Ile115Met) rs1051557 0.00001
NM_003467.3(CXCR4):c.373C>G (p.Leu125Val) rs1001278766 0.00001
NM_003467.3(CXCR4):c.478G>A (p.Val160Ile) rs147198552 0.00001
NM_003467.3(CXCR4):c.516C>A (p.Phe172Leu) rs764678610 0.00001
NM_003467.3(CXCR4):c.586G>A (p.Val196Met) rs748098105 0.00001
NM_003467.3(CXCR4):c.727A>C (p.Ile243Leu) rs762937679 0.00001
NM_003467.3(CXCR4):c.747C>A (p.Phe249Leu) rs779760942 0.00001
NM_003467.3(CXCR4):c.1000C>G (p.Arg334Gly) rs104893624
NM_003467.3(CXCR4):c.1001G>C (p.Arg334Pro)
NM_003467.3(CXCR4):c.1011T>G (p.His337Gln)
NM_003467.3(CXCR4):c.103A>G (p.Asn35Asp)
NM_003467.3(CXCR4):c.1042A>G (p.Ser348Gly) rs1573613407
NM_003467.3(CXCR4):c.109A>G (p.Asn37Asp)
NM_003467.3(CXCR4):c.10A>G (p.Ile4Val) rs2104922432
NM_003467.3(CXCR4):c.110A>G (p.Asn37Ser) rs749938835
NM_003467.3(CXCR4):c.116T>C (p.Ile39Thr)
NM_003467.3(CXCR4):c.132del (p.Tyr45fs) rs1684870931
NM_003467.3(CXCR4):c.175G>A (p.Val59Ile)
NM_003467.3(CXCR4):c.184G>A (p.Val62Ile)
NM_003467.3(CXCR4):c.188T>C (p.Met63Thr)
NM_003467.3(CXCR4):c.19T>C (p.Tyr7His) rs560844176
NM_003467.3(CXCR4):c.225del (p.Lys75fs)
NM_003467.3(CXCR4):c.235C>T (p.His79Tyr) rs2104918076
NM_003467.3(CXCR4):c.250G>A (p.Asp84Asn) rs368016542
NM_003467.3(CXCR4):c.256C>T (p.Leu86Phe)
NM_003467.3(CXCR4):c.278T>C (p.Phe93Ser)
NM_003467.3(CXCR4):c.282G>A (p.Trp94Ter) rs2104917984
NM_003467.3(CXCR4):c.295G>A (p.Val99Met)
NM_003467.3(CXCR4):c.305G>A (p.Trp102Ter)
NM_003467.3(CXCR4):c.338A>C (p.His113Pro) rs1684862940
NM_003467.3(CXCR4):c.394C>G (p.Leu132Val)
NM_003467.3(CXCR4):c.415G>A (p.Val139Ile)
NM_003467.3(CXCR4):c.437G>A (p.Arg146Lys)
NM_003467.3(CXCR4):c.458A>C (p.Glu153Ala) rs1553457905
NM_003467.3(CXCR4):c.473T>C (p.Val158Ala)
NM_003467.3(CXCR4):c.475G>A (p.Gly159Ser) rs910532454
NM_003467.3(CXCR4):c.518T>C (p.Ile173Thr)
NM_003467.3(CXCR4):c.560A>G (p.Asp187Gly) rs2104916956
NM_003467.3(CXCR4):c.575A>G (p.Asn192Ser)
NM_003467.3(CXCR4):c.584G>A (p.Trp195Ter)
NM_003467.3(CXCR4):c.591del (p.Val198fs)
NM_003467.3(CXCR4):c.5A>G (p.Glu2Gly)
NM_003467.3(CXCR4):c.650C>A (p.Ser217Tyr) rs1406988415
NM_003467.3(CXCR4):c.653G>C (p.Cys218Ser)
NM_003467.3(CXCR4):c.661A>C (p.Ile221Leu) rs1684851586
NM_003467.3(CXCR4):c.695A>G (p.His232Arg)
NM_003467.3(CXCR4):c.70A>G (p.Met24Val)
NM_003467.3(CXCR4):c.752G>T (p.Cys251Phe) rs2104916053
NM_003467.3(CXCR4):c.804A>T (p.Glu268Asp) rs2104915971
NM_003467.3(CXCR4):c.814C>T (p.Gln272Ter) rs2104915939
NM_003467.3(CXCR4):c.831G>C (p.Glu277Asp) rs2104915918
NM_003467.3(CXCR4):c.865G>A (p.Ala289Thr)
NM_003467.3(CXCR4):c.871G>A (p.Ala291Thr) rs2104915846
NM_003467.3(CXCR4):c.884G>A (p.Cys295Tyr)
NM_003467.3(CXCR4):c.89G>A (p.Arg30His)
NM_003467.3(CXCR4):c.928A>G (p.Lys310Glu) rs1684843543
NM_003467.3(CXCR4):c.964A>G (p.Arg322Gly)
NM_003467.3(CXCR4):c.967G>A (p.Gly323Arg)
NM_003467.3(CXCR4):c.973A>G (p.Ser325Gly) rs1684840650

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