ClinVar Miner

List of variants in gene SLAMF8

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_020125.3(SLAMF8):c.271G>A (p.Gly91Arg) rs148009811 0.00051
NM_020125.3(SLAMF8):c.56C>T (p.Thr19Ile) rs377124328 0.00017
NM_020125.3(SLAMF8):c.777C>G (p.Cys259Trp) rs367765736 0.00013
NM_020125.3(SLAMF8):c.73G>A (p.Val25Met) rs762647287 0.00009
NM_020125.3(SLAMF8):c.413G>A (p.Arg138Lys) rs372242041 0.00005
NM_020125.3(SLAMF8):c.667G>A (p.Glu223Lys) rs149383951 0.00005
NM_020125.3(SLAMF8):c.91G>A (p.Gly31Ser) rs138614766 0.00004
NM_020125.3(SLAMF8):c.496C>T (p.Arg166Trp) rs759722110 0.00002
NM_020125.3(SLAMF8):c.128T>C (p.Phe43Ser) rs769924299 0.00001
NM_020125.3(SLAMF8):c.494G>A (p.Arg165Gln) rs267598116 0.00001
NM_020125.3(SLAMF8):c.650G>T (p.Trp217Leu) rs765154247 0.00001
NM_020125.3(SLAMF8):c.725C>T (p.Ser242Leu) rs548898106 0.00001
NM_020125.3(SLAMF8):c.92G>A (p.Gly31Asp) rs943112449 0.00001
NM_020125.3(SLAMF8):c.119C>G (p.Pro40Arg) rs748211205
NM_020125.3(SLAMF8):c.137G>A (p.Arg46His)
NM_020125.3(SLAMF8):c.217C>T (p.His73Tyr) rs2524925728
NM_020125.3(SLAMF8):c.224G>A (p.Arg75His)
NM_020125.3(SLAMF8):c.235C>G (p.Arg79Gly) rs763656998
NM_020125.3(SLAMF8):c.23G>A (p.Ser8Asn) rs931245451
NM_020125.3(SLAMF8):c.274C>A (p.Pro92Thr)
NM_020125.3(SLAMF8):c.298A>C (p.Asn100His) rs1571134790
NM_020125.3(SLAMF8):c.360G>C (p.Lys120Asn)
NM_020125.3(SLAMF8):c.406G>A (p.Val136Ile) rs866550708
NM_020125.3(SLAMF8):c.436T>G (p.Cys146Gly)
NM_020125.3(SLAMF8):c.475G>A (p.Glu159Lys)
NM_020125.3(SLAMF8):c.497G>T (p.Arg166Leu) rs186733189
NM_020125.3(SLAMF8):c.513C>G (p.Asp171Glu) rs2524945357
NM_020125.3(SLAMF8):c.529C>T (p.His177Tyr)
NM_020125.3(SLAMF8):c.559A>C (p.Ser187Arg)
NM_020125.3(SLAMF8):c.617C>G (p.Pro206Arg)
NM_020125.3(SLAMF8):c.688T>G (p.Ser230Ala)
NM_020125.3(SLAMF8):c.707T>C (p.Leu236Pro) rs747086552
NM_020125.3(SLAMF8):c.709G>C (p.Val237Leu)
NM_020125.3(SLAMF8):c.710T>A (p.Val237Glu) rs776775459
NM_020125.3(SLAMF8):c.95C>T (p.Ser32Leu)

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