ClinVar Miner

List of variants in gene LRIF1 reported as uncertain significance

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_018372.4(LRIF1):c.1483G>A (p.Val495Ile) rs142311156 0.00025
NM_018372.4(LRIF1):c.2201C>T (p.Pro734Leu) rs143295716 0.00024
NM_018372.4(LRIF1):c.419T>C (p.Val140Ala) rs201655335 0.00023
NM_018372.4(LRIF1):c.2246A>G (p.Lys749Arg) rs752661913 0.00015
NM_018372.4(LRIF1):c.1414T>G (p.Leu472Val) rs144476048 0.00007
NM_018372.4(LRIF1):c.1129T>C (p.Ser377Pro) rs762763677 0.00006
NM_018372.4(LRIF1):c.1364C>A (p.Thr455Lys) rs370219260 0.00004
NM_018372.4(LRIF1):c.190A>C (p.Met64Leu) rs770485914 0.00004
NM_018372.4(LRIF1):c.1957A>G (p.Ile653Val) rs371134004 0.00004
NM_018372.4(LRIF1):c.1601A>G (p.His534Arg) rs749424446 0.00003
NM_018372.4(LRIF1):c.211A>G (p.Asn71Asp) rs374234851 0.00003
NM_018372.4(LRIF1):c.2176G>A (p.Glu726Lys) rs542067453 0.00003
NM_018372.4(LRIF1):c.1222T>G (p.Ser408Ala) rs760912518 0.00002
NM_018372.4(LRIF1):c.53G>A (p.Gly18Asp) rs376985715 0.00002
NM_018372.4(LRIF1):c.1360A>G (p.Thr454Ala) rs956679461 0.00001
NM_018372.4(LRIF1):c.2014A>G (p.Thr672Ala) rs775682328 0.00001
NM_018372.4(LRIF1):c.316T>G (p.Tyr106Asp) rs763115833 0.00001
NM_018372.4(LRIF1):c.784A>G (p.Ile262Val) rs1172401322 0.00001
NM_018372.4(LRIF1):c.1012A>G (p.Ser338Gly)
NM_018372.4(LRIF1):c.1013G>A (p.Ser338Asn)
NM_018372.4(LRIF1):c.101C>G (p.Thr34Arg)
NM_018372.4(LRIF1):c.1049T>C (p.Met350Thr)
NM_018372.4(LRIF1):c.1094A>G (p.Tyr365Cys)
NM_018372.4(LRIF1):c.1114A>G (p.Thr372Ala)
NM_018372.4(LRIF1):c.1151C>A (p.Ser384Tyr)
NM_018372.4(LRIF1):c.1207C>A (p.Pro403Thr) rs2524379255
NM_018372.4(LRIF1):c.1219A>C (p.Ile407Leu) rs200821921
NM_018372.4(LRIF1):c.1285C>T (p.Leu429Phe)
NM_018372.4(LRIF1):c.1376T>G (p.Met459Arg)
NM_018372.4(LRIF1):c.1387A>G (p.Ser463Gly)
NM_018372.4(LRIF1):c.1406G>A (p.Ser469Asn)
NM_018372.4(LRIF1):c.1435C>A (p.Pro479Thr)
NM_018372.4(LRIF1):c.148A>C (p.Lys50Gln) rs1285430292
NM_018372.4(LRIF1):c.1538C>T (p.Ser513Phe)
NM_018372.4(LRIF1):c.1547C>A (p.Ala516Glu) rs768144996
NM_018372.4(LRIF1):c.1547C>G (p.Ala516Gly) rs768144996
NM_018372.4(LRIF1):c.1584C>A (p.Asp528Glu)
NM_018372.4(LRIF1):c.1677T>G (p.Asn559Lys)
NM_018372.4(LRIF1):c.1796C>G (p.Ser599Cys)
NM_018372.4(LRIF1):c.1832A>G (p.Glu611Gly)
NM_018372.4(LRIF1):c.1843A>G (p.Met615Val)
NM_018372.4(LRIF1):c.1908G>T (p.Lys636Asn)
NM_018372.4(LRIF1):c.1919A>G (p.His640Arg) rs2524364945
NM_018372.4(LRIF1):c.1976A>T (p.Asn659Ile) rs374381226
NM_018372.4(LRIF1):c.2174C>T (p.Thr725Ile) rs775310244
NM_018372.4(LRIF1):c.2262G>C (p.Glu754Asp) rs1239009766
NM_018372.4(LRIF1):c.2275C>A (p.Leu759Ile) rs2524362660
NM_018372.4(LRIF1):c.2288G>A (p.Arg763His)
NM_018372.4(LRIF1):c.22G>A (p.Val8Ile)
NM_018372.4(LRIF1):c.239T>A (p.Phe80Tyr)
NM_018372.4(LRIF1):c.266C>G (p.Thr89Arg) rs766273687
NM_018372.4(LRIF1):c.317A>T (p.Tyr106Phe) rs775748979
NM_018372.4(LRIF1):c.428A>G (p.Asp143Gly)
NM_018372.4(LRIF1):c.58G>T (p.Ala20Ser)
NM_018372.4(LRIF1):c.632C>A (p.Ala211Glu) rs369628997
NM_018372.4(LRIF1):c.643A>T (p.Thr215Ser)
NM_018372.4(LRIF1):c.656G>T (p.Gly219Val)
NM_018372.4(LRIF1):c.70G>A (p.Val24Ile)
NM_018372.4(LRIF1):c.724G>A (p.Val242Ile) rs983788342
NM_018372.4(LRIF1):c.739C>A (p.Gln247Lys)
NM_018372.4(LRIF1):c.761T>C (p.Val254Ala) rs1177282415
NM_018372.4(LRIF1):c.821C>T (p.Thr274Ile)
NM_018372.4(LRIF1):c.934A>G (p.Asn312Asp)

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