ClinVar Miner

List of variants in gene RAB11FIP5 reported as uncertain significance

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Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_001371272.1(RAB11FIP5):c.709C>T (p.Arg237Cys) rs759424713 0.00066
NM_001371272.1(RAB11FIP5):c.806G>C (p.Gly269Ala) rs144852010 0.00014
NM_001371272.1(RAB11FIP5):c.1088C>T (p.Pro363Leu) rs201939228 0.00013
NM_001371272.1(RAB11FIP5):c.1355G>C (p.Gly452Ala) rs200575843 0.00013
NM_001371272.1(RAB11FIP5):c.1279C>T (p.Arg427Trp) rs536535862 0.00011
NM_001371272.1(RAB11FIP5):c.731C>G (p.Ser244Cys) rs146810561 0.00008
NM_001371272.1(RAB11FIP5):c.1285C>T (p.Pro429Ser) rs145839919 0.00006
NM_001371272.1(RAB11FIP5):c.1558C>A (p.Gln520Lys) rs774406646 0.00006
NM_001371272.1(RAB11FIP5):c.1442G>A (p.Ser481Asn) rs201625360 0.00005
NM_001371272.1(RAB11FIP5):c.1454A>G (p.Glu485Gly) rs774600602 0.00005
NM_001371272.1(RAB11FIP5):c.1361G>A (p.Arg454Gln) rs775520238 0.00004
NM_001371272.1(RAB11FIP5):c.1063C>T (p.Arg355Cys) rs538411572 0.00003
NM_001371272.1(RAB11FIP5):c.745A>G (p.Asn249Asp) rs751147116 0.00003
NM_001371272.1(RAB11FIP5):c.829C>T (p.Arg277Cys) rs764178093 0.00003
NM_001371272.1(RAB11FIP5):c.974A>G (p.Gln325Arg) rs769496407 0.00003
NM_001371272.1(RAB11FIP5):c.1439G>A (p.Arg480Gln) rs138258802 0.00002
NM_001371272.1(RAB11FIP5):c.1553C>T (p.Pro518Leu) rs373507575 0.00002
NM_001371272.1(RAB11FIP5):c.721C>T (p.Arg241Cys) rs768928394 0.00002
NM_001371272.1(RAB11FIP5):c.749C>A (p.Thr250Asn) rs763683535 0.00002
NM_001371272.1(RAB11FIP5):c.955C>T (p.Arg319Trp) rs1018244205 0.00002
NM_001371272.1(RAB11FIP5):c.1048G>T (p.Gly350Cys) rs1237247948 0.00001
NM_001371272.1(RAB11FIP5):c.1049G>T (p.Gly350Val) rs774750146 0.00001
NM_001371272.1(RAB11FIP5):c.1306G>T (p.Val436Phe) rs1245888622 0.00001
NM_001371272.1(RAB11FIP5):c.1421G>A (p.Arg474Gln) rs1278376687 0.00001
NM_001371272.1(RAB11FIP5):c.299C>T (p.Ala100Val) rs748867084 0.00001
NM_001371272.1(RAB11FIP5):c.319G>A (p.Glu107Lys) rs757003817 0.00001
NM_001371272.1(RAB11FIP5):c.32C>T (p.Ala11Val) rs762477096 0.00001
NM_001371272.1(RAB11FIP5):c.3631G>A (p.Asp1211Asn) rs764184258 0.00001
NM_001371272.1(RAB11FIP5):c.991G>A (p.Ala331Thr) rs146801309 0.00001
NM_001371272.1(RAB11FIP5):c.1022G>T (p.Ser341Ile) rs1194809255
NM_001371272.1(RAB11FIP5):c.1052C>T (p.Pro351Leu) rs1684140658
NM_001371272.1(RAB11FIP5):c.1057C>T (p.Arg353Trp)
NM_001371272.1(RAB11FIP5):c.1111G>A (p.Val371Ile) rs757499419
NM_001371272.1(RAB11FIP5):c.1121G>A (p.Arg374Gln)
NM_001371272.1(RAB11FIP5):c.1188C>G (p.Ser396Arg)
NM_001371272.1(RAB11FIP5):c.1249G>T (p.Ala417Ser) rs1684133920
NM_001371272.1(RAB11FIP5):c.1290G>C (p.Glu430Asp)
NM_001371272.1(RAB11FIP5):c.144C>G (p.Ile48Met)
NM_001371272.1(RAB11FIP5):c.1535T>G (p.Leu512Trp)
NM_001371272.1(RAB11FIP5):c.259C>T (p.Arg87Trp) rs112480158
NM_001371272.1(RAB11FIP5):c.292T>C (p.Trp98Arg) rs1684683632
NM_001371272.1(RAB11FIP5):c.29C>T (p.Ala10Val) rs2529644647
NM_001371272.1(RAB11FIP5):c.355G>A (p.Gly119Ser)
NM_001371272.1(RAB11FIP5):c.3583C>T (p.Pro1195Ser)
NM_001371272.1(RAB11FIP5):c.3601C>T (p.Leu1201Phe)
NM_001371272.1(RAB11FIP5):c.3610G>A (p.Ala1204Thr)
NM_001371272.1(RAB11FIP5):c.3700A>T (p.Thr1234Ser)
NM_001371272.1(RAB11FIP5):c.3868C>T (p.Arg1290Trp) rs1395259449
NM_001371272.1(RAB11FIP5):c.38C>G (p.Pro13Arg) rs765022624
NM_001371272.1(RAB11FIP5):c.3907C>T (p.Arg1303Trp)
NM_001371272.1(RAB11FIP5):c.3962G>T (p.Gly1321Val) rs745917151
NM_001371272.1(RAB11FIP5):c.3968C>G (p.Pro1323Arg) rs201350069
NM_001371272.1(RAB11FIP5):c.424C>A (p.His142Asn)
NM_001371272.1(RAB11FIP5):c.478G>A (p.Gly160Ser) rs2529606214
NM_001371272.1(RAB11FIP5):c.483G>T (p.Glu161Asp)
NM_001371272.1(RAB11FIP5):c.499C>G (p.Gln167Glu)
NM_001371272.1(RAB11FIP5):c.506C>T (p.Thr169Met)
NM_001371272.1(RAB11FIP5):c.52C>T (p.Pro18Ser) rs2529644567
NM_001371272.1(RAB11FIP5):c.530T>C (p.Met177Thr) rs774011431
NM_001371272.1(RAB11FIP5):c.550G>A (p.Asp184Asn)
NM_001371272.1(RAB11FIP5):c.643A>G (p.Ser215Gly)
NM_001371272.1(RAB11FIP5):c.66G>C (p.Gln22His)
NM_001371272.1(RAB11FIP5):c.722G>A (p.Arg241His)
NM_001371272.1(RAB11FIP5):c.752C>T (p.Ser251Leu)
NM_001371272.1(RAB11FIP5):c.786C>A (p.Ser262Arg)
NM_001371272.1(RAB11FIP5):c.788G>A (p.Gly263Glu) rs142965971
NM_001371272.1(RAB11FIP5):c.788G>C (p.Gly263Ala) rs142965971
NM_001371272.1(RAB11FIP5):c.830G>A (p.Arg277His) rs372149039
NM_001371272.1(RAB11FIP5):c.830G>T (p.Arg277Leu) rs372149039
NM_001371272.1(RAB11FIP5):c.842G>A (p.Arg281His)
NM_001371272.1(RAB11FIP5):c.85C>T (p.Arg29Cys)
NM_001371272.1(RAB11FIP5):c.864A>C (p.Glu288Asp) rs772677659

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