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20 records found for search term Hlf
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15105774CV715571single nucleotide variantNM_002126.5(HLF):c.75G>A (p.Leu25=)not provided [RCV000959950]benign175526555955265559Humanname
598179007CV3975288single nucleotide variantNM_002126.5(HLF):c.25C>T (p.Pro9Ser)not specified [RCV005352080]uncertain significance175526550955265509Humanname
155925365CV2230418single nucleotide variantNM_002126.5(HLF):c.86C>T (p.Pro29Leu)not specified [RCV004095874]uncertain significance175526557055265570Humanname
156141104CV2247203single nucleotide variantNM_002126.5(HLF):c.56A>G (p.Tyr19Cys)not specified [RCV004114721]uncertain significance175526554055265540Humanname
9686907CV171604duplicationNM_002126.5(HLF):c.436dup (p.Ser146fs)Prostate cancer [RCV000149126]uncertain significance175526807055268071Human2name
401864294CV2767594single nucleotide variantNM_002126.5(HLF):c.103C>T (p.His35Tyr)not specified [RCV004343740]uncertain significance175526558755265587Humanname
405790589CV3266734single nucleotide variantNM_002126.5(HLF):c.133G>A (p.Asp45Asn)not specified [RCV004399557]uncertain significance175526776855267768Humanname
405790593CV3266735single nucleotide variantNM_002126.5(HLF):c.258G>T (p.Met86Ile)not specified [RCV004399558]uncertain significance175526789355267893Humanname
156387001CV2221376single nucleotide variantNM_002126.5(HLF):c.728G>A (p.Arg243His)not specified [RCV004096676]uncertain significance175532071955320719Humanname
155927680CV2230827single nucleotide variantNM_002126.5(HLF):c.631A>T (p.Ile211Phe)not specified [RCV004092041]uncertain significance175531540655315406Humanname
156240976CV2246052single nucleotide variantNM_002126.5(HLF):c.593G>A (p.Arg198His)not specified [RCV004113965]uncertain significance175531536855315368Humanname
155925113CV2248952single nucleotide variantNM_002126.5(HLF):c.385C>T (p.Arg129Trp)not specified [RCV004115952]uncertain significance175526802055268020Humanname
156280918CV2321735single nucleotide variantNM_002126.5(HLF):c.528G>C (p.Glu176Asp)not specified [RCV004179730]uncertain significance175531530355315303Humanname
156156828CV2359886single nucleotide variantNM_002126.5(HLF):c.448C>G (p.Pro150Ala)not specified [RCV004212737]uncertain significance175526808355268083Humanname
329394432CV2461347single nucleotide variantNM_002126.5(HLF):c.472C>T (p.Arg158Cys)not specified [RCV004267508]uncertain significance175531524755315247Humanname
329399453CV2470104single nucleotide variantNM_002126.5(HLF):c.633C>G (p.Ile211Met)not specified [RCV004287362]uncertain significance175531540855315408Humanname
405790596CV3266736single nucleotide variantNM_002126.5(HLF):c.335G>T (p.Gly112Val)not specified [RCV004399559]uncertain significance175526797055267970Humanname
407527521CV3433587single nucleotide variantNM_002126.5(HLF):c.574A>G (p.Met192Val)not specified [RCV004632822]uncertain significance175531534955315349Humanname
597790919CV3682676single nucleotide variantNM_002126.5(HLF):c.386G>A (p.Arg129Gln)not specified [RCV004933336]uncertain significance175526802155268021Humanname
598179013CV3975289single nucleotide variantNM_002126.5(HLF):c.539C>G (p.Ala180Gly)not specified [RCV005352081]uncertain significance175531531455315314Humanname