ClinVar Miner

List of variants in gene SLX4 reported as likely benign by Sema4, Sema4

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Gene type:
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_032444.4(SLX4):c.5501A>G (p.Asn1834Ser) rs111738042 0.00575
NM_032444.4(SLX4):c.4241C>T (p.Pro1414Leu) rs140892471 0.00307
NM_032444.4(SLX4):c.2290C>G (p.Pro764Ala) rs151105762 0.00218
NM_032444.4(SLX4):c.4648C>T (p.Arg1550Trp) rs77021998 0.00214
NM_032444.4(SLX4):c.2103G>C (p.Glu701Asp) rs73505420 0.00210
NM_032444.4(SLX4):c.2328-9G>C rs73505419 0.00188
NM_032444.4(SLX4):c.422G>T (p.Gly141Val) rs77306735 0.00131
NM_032444.4(SLX4):c.2359G>A (p.Glu787Lys) rs140600202 0.00125
NM_032444.4(SLX4):c.4479G>A (p.Ser1493=) rs150097733 0.00112
NM_032444.4(SLX4):c.2047G>A (p.Ala683Thr) rs115866745 0.00092
NM_032444.4(SLX4):c.1372A>G (p.Lys458Glu) rs149126845 0.00087
NM_032444.4(SLX4):c.3774C>T (p.Pro1258=) rs146054214 0.00085
NM_032444.4(SLX4):c.85C>T (p.Arg29Cys) rs144832924 0.00078
NM_032444.4(SLX4):c.2667A>G (p.Gln889=) rs146790631 0.00066
NM_032444.4(SLX4):c.339T>C (p.Ser113=) rs144326379 0.00061
NM_032444.4(SLX4):c.2844G>A (p.Ala948=) rs376877866 0.00053
NM_032444.4(SLX4):c.4836C>T (p.Asp1612=) rs140844106 0.00051
NM_032444.4(SLX4):c.3189C>T (p.Gly1063=) rs200742809 0.00047
NM_032444.4(SLX4):c.1707G>A (p.Pro569=) rs141687678 0.00044
NM_032444.4(SLX4):c.5248G>T (p.Ala1750Ser) rs771897046 0.00035
NM_032444.4(SLX4):c.1470C>T (p.Leu490=) rs139766312 0.00031
NM_032444.4(SLX4):c.86G>A (p.Arg29His) rs149117119 0.00026
NM_032444.4(SLX4):c.1389A>G (p.Lys463=) rs376668879 0.00019
NM_032444.4(SLX4):c.3583_3585del (p.Ile1195del) rs199897550 0.00019
NM_032444.4(SLX4):c.5433C>T (p.Ala1811=) rs142477564 0.00017
NM_032444.4(SLX4):c.5249C>T (p.Ala1750Val) rs745421287 0.00015
NM_032444.4(SLX4):c.1925-13A>T rs201324113 0.00011
NM_032444.4(SLX4):c.833G>A (p.Arg278Gln) rs201192909 0.00011
NM_032444.4(SLX4):c.1602C>T (p.Ser534=) rs201754095 0.00010
NM_032444.4(SLX4):c.1911G>T (p.Ser637=) rs200013924 0.00010
NM_032444.4(SLX4):c.1701C>T (p.Pro567=) rs776750571 0.00007
NM_032444.4(SLX4):c.3762G>A (p.Ser1254=) rs3810814 0.00007
NM_032444.4(SLX4):c.4344C>T (p.Pro1448=) rs368388100 0.00007
NM_032444.4(SLX4):c.2949C>T (p.Tyr983=) rs758944750 0.00006
NM_032444.4(SLX4):c.4530G>T (p.Leu1510=) rs139254595 0.00006
NM_032444.4(SLX4):c.162C>A (p.Leu54=) rs776979024 0.00004
NM_032444.4(SLX4):c.1662C>T (p.Leu554=) rs375996119 0.00004
NM_032444.4(SLX4):c.2346C>T (p.Leu782=) rs775150046 0.00004
NM_032444.4(SLX4):c.2490G>A (p.Ala830=) rs753595071 0.00004
NM_032444.4(SLX4):c.3042G>A (p.Arg1014=) rs752948857 0.00003
NM_032444.4(SLX4):c.4185C>T (p.Val1395=) rs993089915 0.00003
NM_032444.4(SLX4):c.4485G>C (p.Ala1495=) rs140872903 0.00003
NM_032444.4(SLX4):c.4686G>T (p.Pro1562=) rs752013105 0.00003
NM_032444.4(SLX4):c.1404C>G (p.Pro468=) rs765351696 0.00002
NM_032444.4(SLX4):c.2169T>C (p.Asn723=) rs750908864 0.00002
NM_032444.4(SLX4):c.2166C>T (p.Asn722=) rs767528538 0.00001
NM_032444.4(SLX4):c.2412A>G (p.Glu804=) rs753755892 0.00001
NM_032444.4(SLX4):c.2517C>T (p.His839=) rs766929821 0.00001
NM_032444.4(SLX4):c.3064C>T (p.Leu1022=) rs1391997347 0.00001
NM_032444.4(SLX4):c.4947A>G (p.Thr1649=) rs540634044 0.00001
NM_032444.4(SLX4):c.1329G>A (p.Leu443=) rs2151131782
NM_032444.4(SLX4):c.1887C>T (p.Pro629=) rs762862604
NM_032444.4(SLX4):c.1929G>A (p.Leu643=) rs778062467
NM_032444.4(SLX4):c.1965T>C (p.Phe655=) rs2151129331
NM_032444.4(SLX4):c.2223T>G (p.Gly741=) rs777278153
NM_032444.4(SLX4):c.2721G>A (p.Glu907=) rs141450907
NM_032444.4(SLX4):c.3180G>A (p.Arg1060=) rs747169328
NM_032444.4(SLX4):c.3654T>C (p.Asp1218=) rs2151123167
NM_032444.4(SLX4):c.396A>G (p.Glu132=) rs2151139288
NM_032444.4(SLX4):c.4020C>T (p.His1340=) rs768829231
NM_032444.4(SLX4):c.4596C>T (p.Ser1532=) rs527733303
NM_032444.4(SLX4):c.4845G>A (p.Gln1615=) rs988625732
NM_032444.4(SLX4):c.5166T>C (p.Cys1722=) rs1198701950
NM_032444.4(SLX4):c.5253C>T (p.Asp1751=) rs748978984

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