ClinVar Miner

List of variants in gene CXCR4 reported as likely benign for Warts, hypogammaglobulinemia, infections, and myelokathexis

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_003467.3(CXCR4):c.708G>A (p.Lys236=) rs199713103 0.00036
NM_003467.3(CXCR4):c.153T>A (p.Thr51=) rs145879963 0.00021
NM_003467.3(CXCR4):c.294C>T (p.Ala98=) rs142289207 0.00021
NM_003467.3(CXCR4):c.861C>T (p.Thr287=) rs535778934 0.00016
NM_003467.3(CXCR4):c.676C>T (p.Leu226=) rs180746866 0.00011
NM_003467.3(CXCR4):c.1003G>A (p.Gly335Ser) rs147214773 0.00008
NM_003467.3(CXCR4):c.219G>A (p.Thr73=) rs909200339 0.00005
NM_003467.3(CXCR4):c.87C>T (p.Phe29=) rs768296315 0.00004
NM_003467.3(CXCR4):c.420C>T (p.His140=) rs774159824 0.00003
NM_003467.3(CXCR4):c.249C>T (p.Ala83=) rs1013459896 0.00002
NM_003467.3(CXCR4):c.270G>A (p.Thr90=) rs753770848 0.00002
NM_003467.3(CXCR4):c.15+18C>T rs774545896 0.00001
NM_003467.3(CXCR4):c.16-24T>C rs776615103 0.00001
NM_003467.3(CXCR4):c.39C>G (p.Thr13=) rs375868851 0.00001
NM_003467.3(CXCR4):c.477C>T (p.Gly159=) rs1259138331 0.00001
NM_003467.3(CXCR4):c.528C>T (p.Asn176=) rs113338664 0.00001
NM_003467.3(CXCR4):c.1008A>G (p.Gly336=)
NM_003467.3(CXCR4):c.1026T>C (p.Thr342=) rs2104915514
NM_003467.3(CXCR4):c.1032T>C (p.Ser344=) rs758871604
NM_003467.3(CXCR4):c.15+7C>T rs2104922411
NM_003467.3(CXCR4):c.15+9A>C rs2104922408
NM_003467.3(CXCR4):c.165C>A (p.Gly55=)
NM_003467.3(CXCR4):c.228C>T (p.Tyr76=)
NM_003467.3(CXCR4):c.267C>T (p.Ile89=)
NM_003467.3(CXCR4):c.273T>C (p.Leu91=) rs1025484081
NM_003467.3(CXCR4):c.307T>C (p.Tyr103His)
NM_003467.3(CXCR4):c.30T>C (p.Asp10=) rs1245012855
NM_003467.3(CXCR4):c.342C>A (p.Val114=)
NM_003467.3(CXCR4):c.363C>T (p.Tyr121=)
NM_003467.3(CXCR4):c.39C>T (p.Thr13=)
NM_003467.3(CXCR4):c.402C>A (p.Arg134=) rs2104917808
NM_003467.3(CXCR4):c.438G>A (p.Arg146=)
NM_003467.3(CXCR4):c.444G>A (p.Arg148=)
NM_003467.3(CXCR4):c.453G>A (p.Leu151=)
NM_003467.3(CXCR4):c.501G>A (p.Leu167=)
NM_003467.3(CXCR4):c.504T>A (p.Thr168=)
NM_003467.3(CXCR4):c.549A>G (p.Arg183=)
NM_003467.3(CXCR4):c.552T>C (p.Tyr184=)
NM_003467.3(CXCR4):c.624T>C (p.Leu208=)
NM_003467.3(CXCR4):c.660C>T (p.Cys220=) rs2104916277
NM_003467.3(CXCR4):c.747C>T (p.Phe249=) rs779760942
NM_003467.3(CXCR4):c.795C>T (p.Ile265=)
NM_003467.3(CXCR4):c.798C>T (p.Leu266=)
NM_003467.3(CXCR4):c.7G>T (p.Gly3Trp)
NM_003467.3(CXCR4):c.843C>T (p.His281=)
NM_003467.3(CXCR4):c.862G>A (p.Glu288Lys)
NM_003467.3(CXCR4):c.870A>G (p.Leu290=) rs1573613626
NM_003467.3(CXCR4):c.912C>T (p.Phe304=)
NM_003467.3(CXCR4):c.933C>G (p.Thr311=)
NM_003467.3(CXCR4):c.957T>G (p.Ser319=)
NM_003467.3(CXCR4):c.984C>A (p.Ile328=)

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