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Variants search result for Homo sapiens
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50 records found for search term Hus1b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407480347CV3444265single nucleotide variantNM_148959.4(HUS1B):c.5A>C (p.Lys2Thr)not specified [RCV004635361]uncertain significance6656940656940Humanname
598129024CV3886827single nucleotide variantNM_148959.4(HUS1B):c.219A>G (p.Glu73=)not provided [RCV005244487]likely benign6656726656726Humanname
15182476CV735728single nucleotide variantNM_148959.4(HUS1B):c.264C>T (p.Ser88=)not provided [RCV000907829]benign6656681656681Humanname
156397844CV2193807single nucleotide variantNM_148959.4(HUS1B):c.53A>C (p.His18Pro)not specified [RCV004074559]uncertain significance6656892656892Humanname
156139702CV2280767single nucleotide variantNM_148959.4(HUS1B):c.29A>G (p.Lys10Arg)not specified [RCV004145032]uncertain significance6656916656916Humanname
156286602CV2360935single nucleotide variantNM_148959.4(HUS1B):c.98G>A (p.Arg33His)not specified [RCV004215748]uncertain significance6656847656847Humanname
155987989CV2363915single nucleotide variantNM_148959.4(HUS1B):c.35G>C (p.Cys12Ser)not specified [RCV004218886]uncertain significance6656910656910Humanname
329370988CV2431832single nucleotide variantNM_148959.4(HUS1B):c.53A>T (p.His18Leu)not specified [RCV004254974]uncertain significance6656892656892Humanname
405780202CV3270749single nucleotide variantNM_148959.4(HUS1B):c.70G>A (p.Ala24Thr)not specified [RCV004397478]uncertain significance6656875656875Humanname
597783479CV3686264single nucleotide variantNM_148959.4(HUS1B):c.97C>T (p.Arg33Cys)not specified [RCV004931428]uncertain significance6656848656848Humanname
597783945CV3686267single nucleotide variantNM_148959.4(HUS1B):c.67G>A (p.Val23Ile)not specified [RCV004931431]uncertain significance6656878656878Humanname
156373959CV2198108single nucleotide variantNM_148959.4(HUS1B):c.148C>T (p.His50Tyr)not specified [RCV004079703]uncertain significance6656797656797Humanname
155915042CV2264855single nucleotide variantNM_148959.4(HUS1B):c.128C>G (p.Pro43Arg)not specified [RCV004134610]uncertain significance6656817656817Humanname
156041808CV2342173single nucleotide variantNM_148959.4(HUS1B):c.111C>A (p.Asp37Glu)not specified [RCV004191761]uncertain significance6656834656834Humanname
156156574CV2359858single nucleotide variantNM_148959.4(HUS1B):c.250G>T (p.Ala84Ser)not specified [RCV004212711]likely benign6656695656695Humanname
401779446CV2676571single nucleotide variantNM_148959.4(HUS1B):c.103C>G (p.Arg35Gly)not specified [RCV004288756]uncertain significance6656842656842Humanname
401896358CV2781127single nucleotide variantNM_148959.4(HUS1B):c.272C>A (p.Ala91Glu)not specified [RCV004352186]uncertain significance6656673656673Humanname
407480357CV3444267single nucleotide variantNM_148959.4(HUS1B):c.279C>G (p.Ser93Arg)not specified [RCV004635363]uncertain significance6656666656666Humanname
597783468CV3686261single nucleotide variantNM_148959.4(HUS1B):c.122T>A (p.Phe41Tyr)not specified [RCV004931425]uncertain significance6656823656823Humanname
597783471CV3686262single nucleotide variantNM_148959.4(HUS1B):c.226G>A (p.Asp76Asn)not specified [RCV004931426]likely benign6656719656719Humanname
597783487CV3686266single nucleotide variantNM_148959.4(HUS1B):c.100G>C (p.Val34Leu)not specified [RCV004931430]uncertain significance6656845656845Humanname
598256792CV3968482single nucleotide variantNM_148959.4(HUS1B):c.228T>G (p.Asp76Glu)not specified [RCV005346868]uncertain significance6656717656717Humanname
155915364CV2200239single nucleotide variantNM_148959.4(HUS1B):c.676A>G (p.Met226Val)not specified [RCV004076582]uncertain significance6656269656269Humanname
156049182CV2241868single nucleotide variantNM_148959.4(HUS1B):c.422T>A (p.Val141Glu)not specified [RCV004106789]uncertain significance6656523656523Humanname
156166431CV2283899single nucleotide variantNM_148959.4(HUS1B):c.464C>G (p.Ala155Gly)not specified [RCV004142402]uncertain significance6656481656481Humanname
155930896CV2297134single nucleotide variantNM_148959.4(HUS1B):c.427C>T (p.Arg143Trp)not specified [RCV004151034]uncertain significance6656518656518Humanname
156053724CV2308598single nucleotide variantNM_148959.4(HUS1B):c.535G>A (p.Val179Met)not specified [RCV004167157]uncertain significance6656410656410Humanname
156108753CV2313814single nucleotide variantNM_148959.4(HUS1B):c.503T>C (p.Ile168Thr)not specified [RCV004164140]uncertain significance6656442656442Humanname
156225451CV2390601single nucleotide variantNM_148959.4(HUS1B):c.769A>G (p.Asn257Asp)not specified [RCV004239126]uncertain significance6656176656176Humanname
156089254CV2392048single nucleotide variantNM_148959.4(HUS1B):c.376C>G (p.Arg126Gly)not specified [RCV004237945]uncertain significance6656569656569Humanname
401751981CV2672641single nucleotide variantNM_148959.4(HUS1B):c.732A>C (p.Gln244His)not specified [RCV004287664]uncertain significance6656213656213Humanname
401739865CV2683190single nucleotide variantNM_148959.4(HUS1B):c.678G>C (p.Met226Ile)not specified [RCV004286186]uncertain significance6656267656267Humanname
401737020CV2689546single nucleotide variantNM_148959.4(HUS1B):c.404G>C (p.Arg135Pro)not specified [RCV004308377]uncertain significance6656541656541Humanname
401746159CV2694803single nucleotide variantNM_148959.4(HUS1B):c.308A>T (p.Gln103Leu)not specified [RCV004298883]uncertain significance6656637656637Humanname
401859716CV2771806single nucleotide variantNM_148959.4(HUS1B):c.439C>T (p.Pro147Ser)not specified [RCV004350573]uncertain significance6656506656506Humanname
405780181CV3270745single nucleotide variantNM_148959.4(HUS1B):c.479C>T (p.Pro160Leu)not specified [RCV004397474]uncertain significance6656466656466Humanname
405780188CV3270746single nucleotide variantNM_148959.4(HUS1B):c.595T>C (p.Ser199Pro)not specified [RCV004397475]uncertain significance6656350656350Humanname
405780192CV3270747single nucleotide variantNM_148959.4(HUS1B):c.631C>A (p.Pro211Thr)not specified [RCV004397476]uncertain significance6656314656314Humanname
405780196CV3270748single nucleotide variantNM_148959.4(HUS1B):c.659A>T (p.Asn220Ile)not specified [RCV004397477]uncertain significance6656286656286Humanname
407480341CV3444264single nucleotide variantNM_148959.4(HUS1B):c.371G>A (p.Arg124His)not specified [RCV004635360]uncertain significance6656574656574Humanname
407480355CV3444266single nucleotide variantNM_148959.4(HUS1B):c.482G>T (p.Arg161Leu)not specified [RCV004635362]uncertain significance6656463656463Humanname
407480363CV3444268single nucleotide variantNM_148959.4(HUS1B):c.762T>G (p.Ile254Met)not specified [RCV004635364]uncertain significance6656183656183Humanname
597783464CV3686260single nucleotide variantNM_148959.4(HUS1B):c.380G>A (p.Ser127Asn)not specified [RCV004931424]uncertain significance6656565656565Humanname
597783475CV3686263single nucleotide variantNM_148959.4(HUS1B):c.428G>A (p.Arg143Gln)not specified [RCV004931427]uncertain significance6656517656517Humanname
597783483CV3686265single nucleotide variantNM_148959.4(HUS1B):c.698A>G (p.Asn233Ser)not specified [RCV004931429]uncertain significance6656247656247Humanname
598256799CV3968483single nucleotide variantNM_148959.4(HUS1B):c.321G>T (p.Lys107Asn)not specified [RCV005346869]uncertain significance6656624656624Humanname
598256804CV3968484single nucleotide variantNM_148959.4(HUS1B):c.664G>T (p.Asp222Tyr)not specified [RCV005346870]uncertain significance6656281656281Humanname
598256809CV3968485single nucleotide variantNM_148959.4(HUS1B):c.484T>G (p.Trp162Gly)not specified [RCV005346871]uncertain significance6656461656461Humanname
15157576CV699642single nucleotide variantNM_148959.4(HUS1B):c.529A>G (p.Ser177Gly)not provided [RCV000946909]benign6656416656416Humanname
15184376CV710584single nucleotide variantNM_148959.4(HUS1B):c.406G>T (p.Val136Leu)not provided [RCV000975098]benign6656539656539Humanname