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Variants search result for Homo sapiens
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21 records found for search term Paqr9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156345182CV2290951single nucleotide variantNM_198504.4(PAQR9):c.4C>T (p.Pro2Ser)not specified [RCV004151507]uncertain significance3142963333142963333Humanname
401748307CV2696347single nucleotide variantNM_198504.4(PAQR9):c.25G>A (p.Gly9Ser)not specified [RCV004312456]uncertain significance3142963312142963312Humanname
15156807CV697868single nucleotide variantNM_198504.4(PAQR9):c.171C>T (p.Cys57=)not provided [RCV000946768]benign3142963166142963166Humanname
155924330CV2211521single nucleotide variantNM_198504.4(PAQR9):c.97G>C (p.Ala33Pro)not specified [RCV004084428]uncertain significance3142963240142963240Humanname
156303194CV2308231single nucleotide variantNM_198504.4(PAQR9):c.61G>A (p.Ala21Thr)not specified [RCV004164731]uncertain significance3142963276142963276Humanname
156169546CV2400492single nucleotide variantNM_198504.4(PAQR9):c.55G>A (p.Ala19Thr)not specified [RCV004246691]likely benign3142963282142963282Humanname
597718496CV3571410single nucleotide variantNM_198504.4(PAQR9):c.74C>T (p.Ala25Val)not specified [RCV004841641]uncertain significance3142963263142963263Humanname
597658463CV3571411single nucleotide variantNM_198504.4(PAQR9):c.47C>T (p.Pro16Leu)not specified [RCV004827718]uncertain significance3142963290142963290Humanname
597658458CV3571412single nucleotide variantNM_198504.4(PAQR9):c.95C>T (p.Ala32Val)not specified [RCV004827719]uncertain significance3142963242142963242Humanname
598259757CV4001984single nucleotide variantNM_198504.4(PAQR9):c.92C>T (p.Ser31Phe)not specified [RCV005386548]uncertain significance3142963245142963245Humanname
15196243CV697867single nucleotide variantNM_198504.4(PAQR9):c.459C>T (p.Phe153=)not provided [RCV000956141]benign3142962878142962878Humanname
156105239CV2307322single nucleotide variantNM_198504.4(PAQR9):c.109C>T (p.Pro37Ser)not specified [RCV004166012]uncertain significance3142963228142963228Humanname
405772110CV3364284single nucleotide variantNM_198504.4(PAQR9):c.191G>A (p.Arg64Gln)not specified [RCV004502469]uncertain significance3142963146142963146Humanname
405772118CV3364285single nucleotide variantNM_198504.4(PAQR9):c.206C>T (p.Thr69Met)not specified [RCV004502470]uncertain significance3142963131142963131Humanname
401894661CV2785145single nucleotide variantNM_198504.4(PAQR9):c.316T>C (p.Phe106Leu)not specified [RCV004355144]uncertain significance3142963021142963021Humanname
401897499CV2787105single nucleotide variantNM_198504.4(PAQR9):c.613C>T (p.Leu205Phe)not specified [RCV004360542]uncertain significance3142962724142962724Humanname
597718479CV3571408single nucleotide variantNM_198504.4(PAQR9):c.554C>G (p.Ala185Gly)not specified [RCV004841639]uncertain significance3142962783142962783Humanname
597718488CV3571409single nucleotide variantNM_198504.4(PAQR9):c.323G>A (p.Ser108Asn)not specified [RCV004841640]uncertain significance3142963014142963014Humanname
597718506CV3571413single nucleotide variantNM_198504.4(PAQR9):c.799C>A (p.Arg267Ser)not specified [RCV004841642]uncertain significance3142962538142962538Humanname
156199705CV2256014single nucleotide variantNM_198504.4(PAQR9):c.1096A>G (p.Lys366Glu)not specified [RCV004122452]uncertain significance3142962241142962241Humanname
156114128CV2349176single nucleotide variantNM_198504.4(PAQR9):c.1034C>G (p.Thr345Ser)not specified [RCV004199135]uncertain significance3142962303142962303Humanname