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Variants search result for Homo sapiens
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38 records found for search term Abcg4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329359516CV2446302single nucleotide variantNM_022169.5(ABCG4):c.14C>T (p.Ala5Val)not specified [RCV004249435]uncertain significance11119149979119149979Humanname
156287689CV2301267single nucleotide variantNM_022169.5(ABCG4):c.82G>A (p.Ala28Thr)not specified [RCV004160447]uncertain significance11119150047119150047Humanname
401772725CV2712876single nucleotide variantNM_022169.5(ABCG4):c.68C>A (p.Thr23Lys)not specified [RCV004314286]uncertain significance11119150033119150033Humanname
598163435CV3995865single nucleotide variantNM_022169.5(ABCG4):c.64G>T (p.Val22Leu)not specified [RCV005390985]uncertain significance11119150029119150029Humanname
15184391CV701605single nucleotide variantNM_022169.5(ABCG4):c.534G>A (p.Lys178=)not provided [RCV000952695]benign11119154569119154569Humanname
9687076CV171499single nucleotide variantNM_022169.5(ABCG4):c.237G>T (p.Arg79Ser)Prostate cancer [RCV000149295]uncertain significance11119150202119150202Human2name
156156179CV2238380single nucleotide variantNM_022169.5(ABCG4):c.281G>A (p.Arg94His)not specified [RCV004113450]uncertain significance11119154068119154068Humanname
597695592CV3574640single nucleotide variantNM_022169.5(ABCG4):c.281G>T (p.Arg94Leu)not specified [RCV004839140]uncertain significance11119154068119154068Humanname
597694419CV3578277single nucleotide variantNM_022169.5(ABCG4):c.284G>A (p.Arg95Gln)not specified [RCV004838975]uncertain significance11119154071119154071Humanname
598162625CV3995696single nucleotide variantNM_022169.5(ABCG4):c.101C>T (p.Thr34Ile)not specified [RCV005390849]uncertain significance11119150066119150066Humanname
15102139CV701606single nucleotide variantNM_022169.5(ABCG4):c.1035C>T (p.Asn345=)not provided [RCV000959235]benign11119156981119156981Humanname
156279096CV2348301single nucleotide variantNM_022169.5(ABCG4):c.759C>G (p.Ile253Met)not specified [RCV004193501]uncertain significance11119156401119156401Humanname
156001466CV2378817single nucleotide variantNM_022169.5(ABCG4):c.461C>T (p.Pro154Leu)not specified [RCV004231261]uncertain significance11119154364119154364Humanname
407525077CV3460966single nucleotide variantNM_022169.5(ABCG4):c.899C>G (p.Pro300Arg)not specified [RCV004653918]uncertain significance11119156652119156652Humanname
597695681CV3574651single nucleotide variantNM_022169.5(ABCG4):c.490G>T (p.Val164Phe)not specified [RCV004839148]uncertain significance11119154525119154525Humanname
598162222CV3995607single nucleotide variantNM_022169.5(ABCG4):c.719T>C (p.Val240Ala)not specified [RCV005390777]uncertain significance11119156361119156361Humanname
598163837CV3995949single nucleotide variantNM_022169.5(ABCG4):c.745G>T (p.Gly249Trp)not specified [RCV005391058]uncertain significance11119156387119156387Humanname
156299255CV2248612single nucleotide variantNM_022169.5(ABCG4):c.1921C>T (p.Arg641Trp)not specified [RCV004121799]uncertain significance11119161086119161086Humanname
155910647CV2303641single nucleotide variantNM_022169.5(ABCG4):c.1205T>C (p.Ile402Thr)not specified [RCV004161722]uncertain significance11119158594119158594Humanname
156334128CV2333343single nucleotide variantNM_022169.5(ABCG4):c.1166C>T (p.Thr389Met)not specified [RCV004190057]uncertain significance11119158331119158331Humanname
156087535CV2336995single nucleotide variantNM_022169.5(ABCG4):c.1243G>A (p.Asp415Asn)not specified [RCV004192766]likely benign11119158632119158632Humanname
156072323CV2365376single nucleotide variantNM_022169.5(ABCG4):c.1273G>A (p.Gly425Ser)not specified [RCV004209457]uncertain significance11119158662119158662Humanname
156135455CV2379887single nucleotide variantNM_022169.5(ABCG4):c.1000G>A (p.Ala334Thr)not specified [RCV004222039]likely benign11119156946119156946Humanname
401766930CV2680196single nucleotide variantNM_022169.5(ABCG4):c.1922G>A (p.Arg641Gln)not specified [RCV004286673]uncertain significance11119161087119161087Humanname
401750689CV2712078single nucleotide variantNM_022169.5(ABCG4):c.1354G>A (p.Val452Ile)not specified [RCV004311816]uncertain significance11119158846119158846Humanname
401864502CV2777864single nucleotide variantNM_022169.5(ABCG4):c.1799G>A (p.Arg600Gln)not specified [RCV004347838]likely benign11119160964119160964Humanname
405663330CV3290237single nucleotide variantNM_022169.5(ABCG4):c.1039G>A (p.Val347Ile)not specified [RCV004418010]uncertain significance11119156985119156985Humanname
405663389CV3290249single nucleotide variantNM_022169.5(ABCG4):c.1468G>A (p.Val490Met)not specified [RCV004418022]uncertain significance11119160257119160257Humanname
405663681CV3290253single nucleotide variantNM_022169.5(ABCG4):c.1532C>T (p.Thr511Ile)not specified [RCV004418026]uncertain significance11119160321119160321Humanname
597695535CV3574626single nucleotide variantNM_022169.5(ABCG4):c.1711G>A (p.Val571Ile)not specified [RCV004839134]uncertain significance11119160652119160652Humanname
597695766CV3574702single nucleotide variantNM_022169.5(ABCG4):c.1660A>G (p.Ser554Gly)not specified [RCV004839157]uncertain significance11119160601119160601Humanname
597694644CV3578364single nucleotide variantNM_022169.5(ABCG4):c.1210G>A (p.Val404Met)not specified [RCV004839024]uncertain significance11119158599119158599Humanname
597695098CV3578467single nucleotide variantNM_022169.5(ABCG4):c.1359C>G (p.Phe453Leu)not specified [RCV004839094]uncertain significance11119158851119158851Humanname
598163079CV3995785single nucleotide variantNM_022169.5(ABCG4):c.1732G>A (p.Val578Met)not specified [RCV005390926]uncertain significance11119160897119160897Humanname
598268402CV3998851single nucleotide variantNM_022169.5(ABCG4):c.1573G>A (p.Gly525Arg)not specified [RCV005388583]uncertain significance11119160362119160362Humanname
598268754CV3998934single nucleotide variantNM_022169.5(ABCG4):c.1360A>T (p.Met454Leu)not specified [RCV005388652]uncertain significance11119158852119158852Humanname
598161881CV3999023single nucleotide variantNM_022169.5(ABCG4):c.1448C>T (p.Pro483Leu)not specified [RCV005390708]uncertain significance11119160237119160237Humanname
15102145CV701607single nucleotide variantNM_022169.5(ABCG4):c.1055C>T (p.Pro352Leu)not provided [RCV000959236]benign11119157001119157001Humanname