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Variants search result for Homo sapiens
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48 records found for search term Bin3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15197812CV777696single nucleotide variantNM_018688.6(BIN3):c.297+5C>Tnot provided [RCV000956570]benign82263043722630437Humanname
598247947CV3949510single nucleotide variantNM_018688.6(BIN3):c.4A>T (p.Ser2Cys)not specified [RCV005297951]uncertain significance82266904822669048Humanname
155947469CV2262682single nucleotide variantNM_018688.6(BIN3):c.92T>C (p.Leu31Pro)not specified [RCV004130875]uncertain significance82263692822636928Humanname
598161421CV3949509single nucleotide variantNM_018688.6(BIN3):c.56C>T (p.Thr19Ile)not specified [RCV005307004]uncertain significance82264475622644756Humanname
156346851CV2300747single nucleotide variantNM_018688.6(BIN3):c.184A>T (p.Ile62Leu)not specified [RCV004155680]uncertain significance82263055522630555Humanname
156004068CV2396861single nucleotide variantNM_018688.6(BIN3):c.215G>A (p.Cys72Tyr)not specified [RCV004233989]uncertain significance82263052422630524Humanname
329370368CV2435560single nucleotide variantNM_018688.6(BIN3):c.272G>C (p.Arg91Pro)not specified [RCV004254816]uncertain significance82263046722630467Humanname
329399476CV2436163single nucleotide variantNM_018688.6(BIN3):c.206A>G (p.Asn69Ser)not specified [RCV004249796]uncertain significance82263053322630533Humanname
329396279CV2462481single nucleotide variantNM_018688.6(BIN3):c.208C>T (p.Pro70Ser)not specified [RCV004276661]uncertain significance82263053122630531Humanname
401742759CV2677672single nucleotide variantNM_018688.6(BIN3):c.276G>A (p.Met92Ile)not specified [RCV004291758]uncertain significance82263046322630463Humanname
407473149CV3427657single nucleotide variantNM_018688.6(BIN3):c.167C>T (p.Ser56Leu)not specified [RCV004600293]uncertain significance82263057222630572Humanname
407473153CV3427658single nucleotide variantNM_018688.6(BIN3):c.287A>G (p.Asn96Ser)not specified [RCV004600294]uncertain significance82263045222630452Humanname
598247954CV3949511single nucleotide variantNM_018688.6(BIN3):c.203C>T (p.Ser68Phe)not specified [RCV005297952]uncertain significance82263053622630536Humanname
598247961CV3949512single nucleotide variantNM_018688.6(BIN3):c.248C>T (p.Thr83Met)not specified [RCV005297953]uncertain significance82263049122630491Humanname
598247975CV3949514single nucleotide variantNM_018688.6(BIN3):c.111G>T (p.Gln37His)not specified [RCV005297955]uncertain significance82263657422636574Humanname
598161426CV3949515single nucleotide variantNM_018688.6(BIN3):c.132C>G (p.Asp44Glu)not specified [RCV005307005]uncertain significance82263655322636553Humanname
598161442CV3949521single nucleotide variantNM_018688.6(BIN3):c.148G>A (p.Asp50Asn)not specified [RCV005307008]uncertain significance82263653722636537Humanname
156399627CV2202116single nucleotide variantNM_018688.6(BIN3):c.361C>T (p.Leu121Phe)not specified [RCV004078071]uncertain significance82262434122624341Humanname
155901733CV2237772single nucleotide variantNM_018688.6(BIN3):c.551C>T (p.Pro184Leu)not specified [RCV004109021]uncertain significance82262397922623979Humanname
155961670CV2254244single nucleotide variantNM_018688.6(BIN3):c.686C>A (p.Ser229Tyr)not specified [RCV004129920]uncertain significance82262149822621498Humanname
156099573CV2306552single nucleotide variantNM_018688.6(BIN3):c.541G>A (p.Glu181Lys)not specified [RCV004157160]uncertain significance82262398922623989Humanname
156197036CV2306776single nucleotide variantNM_018688.6(BIN3):c.301A>G (p.Asn101Asp)not specified [RCV004159352]uncertain significance82263000122630001Humanname
156290139CV2309790single nucleotide variantNM_018688.6(BIN3):c.629C>T (p.Ser210Leu)not specified [RCV004160910]uncertain significance82262155522621555Humanname
156052919CV2336774single nucleotide variantNM_018688.6(BIN3):c.553C>T (p.Arg185Cys)not specified [RCV004197010]uncertain significance82262397722623977Humanname
156220320CV2345017single nucleotide variantNM_018688.6(BIN3):c.688G>A (p.Asp230Asn)not specified [RCV004193303]uncertain significance82262149622621496Humanname
156106512CV2355252single nucleotide variantNM_018688.6(BIN3):c.391G>C (p.Ala131Pro)not specified [RCV004203105]uncertain significance82262431122624311Humanname
156153088CV2374813single nucleotide variantNM_018688.6(BIN3):c.346A>C (p.Ser116Arg)not specified [RCV004227849]uncertain significance82262435622624356Humanname
156045088CV2381692single nucleotide variantNM_018688.6(BIN3):c.739C>T (p.Leu247Phe)not specified [RCV004232156]uncertain significance82262144522621445Humanname
156344554CV2384891single nucleotide variantNM_018688.6(BIN3):c.608G>A (p.Arg203Gln)not specified [RCV004225766]uncertain significance82262392222623922Humanname
156224651CV2399459single nucleotide variantNM_018688.6(BIN3):c.383G>A (p.Arg128Gln)not specified [RCV004242728]uncertain significance82262431922624319Humanname
329359279CV2435378single nucleotide variantNM_018688.6(BIN3):c.452C>T (p.Thr151Met)not specified [RCV004253033]uncertain significance82262425022624250Humanname
329349775CV2439480single nucleotide variantNM_018688.6(BIN3):c.697C>T (p.Arg233Trp)not specified [RCV004249767]uncertain significance82262148722621487Humanname
401744135CV2677020single nucleotide variantNM_018688.6(BIN3):c.754G>A (p.Asp252Asn)not specified [RCV004293621]uncertain significance82262143022621430Humanname
401781201CV2681925single nucleotide variantNM_018688.6(BIN3):c.662A>G (p.His221Arg)not specified [RCV004296914]uncertain significance82262152222621522Humanname
401764497CV2727964single nucleotide variantNM_018688.6(BIN3):c.574G>T (p.Asp192Tyr)not specified [RCV004324131]uncertain significance82262395622623956Humanname
405730625CV3294580single nucleotide variantNM_018688.6(BIN3):c.549G>A (p.Met183Ile)not specified [RCV004429294]uncertain significance82262398122623981Humanname
405730642CV3294582single nucleotide variantNM_018688.6(BIN3):c.587C>T (p.Pro196Leu)not specified [RCV004429296]uncertain significance82262394322623943Humanname
407473141CV3427653single nucleotide variantNM_018688.6(BIN3):c.499C>G (p.Pro167Ala)not specified [RCV004600289]uncertain significance82262403122624031Humanname
407480413CV3427654single nucleotide variantNM_018688.6(BIN3):c.704G>A (p.Arg235Gln)not specified [RCV004600290]uncertain significance82262148022621480Humanname
407480419CV3427655single nucleotide variantNM_018688.6(BIN3):c.712G>A (p.Glu238Lys)not specified [RCV004600291]uncertain significance82262147222621472Humanname
407500043CV3427659single nucleotide variantNM_018688.6(BIN3):c.311A>G (p.Gln104Arg)not specified [RCV004607047]uncertain significance82262999122629991Humanname
597715378CV3636712single nucleotide variantNM_018688.6(BIN3):c.382C>T (p.Arg128Trp)not specified [RCV004887191]uncertain significance82262432022624320Humanname
597690678CV3636713single nucleotide variantNM_018688.6(BIN3):c.686C>T (p.Ser229Phe)not specified [RCV004887192]uncertain significance82262149822621498Humanname
598161432CV3949516single nucleotide variantNM_018688.6(BIN3):c.508G>A (p.Glu170Lys)not specified [RCV005307006]uncertain significance82262402222624022Humanname
598247982CV3949517single nucleotide variantNM_018688.6(BIN3):c.406A>G (p.Arg136Gly)not specified [RCV005297956]uncertain significance82262429622624296Humanname
598247989CV3949518single nucleotide variantNM_018688.6(BIN3):c.497G>A (p.Arg166Gln)not specified [RCV005297957]uncertain significance82262403322624033Humanname
598247996CV3949519single nucleotide variantNM_018688.6(BIN3):c.667C>G (p.Leu223Val)not specified [RCV005297958]uncertain significance82262151722621517Humanname
598161438CV3949520single nucleotide variantNM_018688.6(BIN3):c.534G>T (p.Gln178His)not specified [RCV005307007]uncertain significance82262399622623996Humanname