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Variants search result for Homo sapiens
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49 records found for search term Ralbp1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15157335CV756589single nucleotide variantNM_006788.4(RALBP1):c.258A>G (p.Ala86=)not provided [RCV000924841]likely benign1895168589516858Humanname
405692629CV3315300single nucleotide variantNM_006788.4(RALBP1):c.45C>A (p.His15Gln)not specified [RCV004445630]uncertain significance1895130909513090Humanname
597753995CV3582571single nucleotide variantNM_006788.4(RALBP1):c.34C>T (p.Pro12Ser)not specified [RCV004847119]uncertain significance1895130799513079Humanname
15194538CV727832single nucleotide variantNM_006788.4(RALBP1):c.894G>A (p.Glu298=)not provided [RCV000889250]likely benign1895223509522350Humanname
155900861CV2298053single nucleotide variantNM_006788.4(RALBP1):c.271G>C (p.Asp91His)not specified [RCV004157946]uncertain significance1895168719516871Humanname
15157339CV756591single nucleotide variantNM_006788.4(RALBP1):c.1923G>A (p.Pro641=)not provided [RCV000924842]likely benign1895358929535892Humanname
15194141CV772272single nucleotide variantNM_006788.4(RALBP1):c.1899G>A (p.Glu633=)not provided [RCV000933559]likely benign1895358689535868Humanname
156301869CV2241686single nucleotide variantNM_006788.4(RALBP1):c.407A>G (p.His136Arg)not specified [RCV004106631]uncertain significance1895170079517007Humanname
155957897CV2282128single nucleotide variantNM_006788.4(RALBP1):c.658G>C (p.Val220Leu)not specified [RCV004138863]uncertain significance1895172589517258Humanname
156362645CV2330287single nucleotide variantNM_006788.4(RALBP1):c.964A>G (p.Ile322Val)not specified [RCV004187733]uncertain significance1895224209522420Humanname
156197390CV2400737single nucleotide variantNM_006788.4(RALBP1):c.584C>G (p.Ala195Gly)not specified [RCV004242405]uncertain significance1895171849517184Humanname
329372031CV2454927single nucleotide variantNM_006788.4(RALBP1):c.914G>T (p.Arg305Leu)not specified [RCV004270417]uncertain significance1895223709522370Humanname
329360824CV2463021single nucleotide variantNM_006788.4(RALBP1):c.982G>A (p.Val328Ile)not specified [RCV004272842]uncertain significance1895224389522438Humanname
401758754CV2705111single nucleotide variantNM_006788.4(RALBP1):c.680G>T (p.Cys227Phe)not specified [RCV004310015]uncertain significance1895172809517280Humanname
405692634CV3315301single nucleotide variantNM_006788.4(RALBP1):c.757A>G (p.Thr253Ala)not specified [RCV004445631]uncertain significance1895222139522213Humanname
407486012CV3472177single nucleotide variantNM_006788.4(RALBP1):c.696A>C (p.Arg232Ser)not specified [RCV004665345]uncertain significance1895172969517296Humanname
597753551CV3582561single nucleotide variantNM_006788.4(RALBP1):c.760A>G (p.Asn254Asp)not specified [RCV004847113]uncertain significance1895222169522216Humanname
597703898CV3582562single nucleotide variantNM_006788.4(RALBP1):c.752A>G (p.Glu251Gly)not specified [RCV004860241]uncertain significance1895222089522208Humanname
597703908CV3582563single nucleotide variantNM_006788.4(RALBP1):c.655T>C (p.Tyr219His)not specified [RCV004860242]uncertain significance1895172559517255Humanname
597703927CV3582565single nucleotide variantNM_006788.4(RALBP1):c.562C>T (p.Pro188Ser)not specified [RCV004860244]uncertain significance1895171629517162Humanname
597753555CV3582566single nucleotide variantNM_006788.4(RALBP1):c.386A>G (p.Glu129Gly)not specified [RCV004847114]uncertain significance1895169869516986Humanname
597754009CV3582567single nucleotide variantNM_006788.4(RALBP1):c.663G>C (p.Glu221Asp)not specified [RCV004847115]uncertain significance1895172639517263Humanname
598174649CV3905204single nucleotide variantNM_006788.4(RALBP1):c.751G>A (p.Glu251Lys)not specified [RCV005263888]uncertain significance1895222079522207Humanname
15141112CV716106single nucleotide variantNM_006788.4(RALBP1):c.623G>A (p.Arg208Gln)not provided [RCV000966253]benign1895172239517223Humanname
15155992CV756590single nucleotide variantNM_006788.4(RALBP1):c.884C>T (p.Thr295Met)not provided [RCV000924577]benign1895223409522340Humanname
156091463CV2216639single nucleotide variantNM_006788.4(RALBP1):c.1637G>A (p.Ser546Asn)not specified [RCV004083096]uncertain significance1895337629533762Humanname
156247180CV2263841single nucleotide variantNM_006788.4(RALBP1):c.1169C>T (p.Thr390Met)not specified [RCV004137901]uncertain significance1895247099524709Humanname
156274485CV2279777single nucleotide variantNM_006788.4(RALBP1):c.1240C>G (p.Arg414Gly)not specified [RCV004144391]uncertain significance1895257449525744Humanname
156135315CV2379865single nucleotide variantNM_006788.4(RALBP1):c.1852G>A (p.Val618Ile)not specified [RCV004219972]uncertain significance1895358219535821Humanname
155902726CV2386323single nucleotide variantNM_006788.4(RALBP1):c.1814C>T (p.Ala605Val)not specified [RCV004228665]likely benign1895357839535783Humanname
329383971CV2434931single nucleotide variantNM_006788.4(RALBP1):c.1859C>T (p.Pro620Leu)not provided [RCV004696338]|not specified [RCV004250801]uncertain significance1895358289535828Humanname
329391571CV2448714single nucleotide variantNM_006788.4(RALBP1):c.1870G>A (p.Gly624Ser)not specified [RCV004259371]likely benign1895358399535839Humanname
401780029CV2676785single nucleotide variantNM_006788.4(RALBP1):c.1765G>A (p.Val589Met)not specified [RCV004290956]uncertain significance1895357349535734Humanname
401746904CV2678953single nucleotide variantNM_006788.4(RALBP1):c.1270T>C (p.Ser424Pro)not specified [RCV004294966]uncertain significance1895257749525774Humanname
401743853CV2684795single nucleotide variantNM_006788.4(RALBP1):c.1804G>A (p.Glu602Lys)not specified [RCV004293870]uncertain significance1895357739535773Humanname
405692601CV3315294single nucleotide variantNM_006788.4(RALBP1):c.1258A>T (p.Ile420Leu)not specified [RCV004445624]uncertain significance1895257629525762Humanname
405692606CV3315295single nucleotide variantNM_006788.4(RALBP1):c.1513C>T (p.Arg505Trp)not specified [RCV004445625]uncertain significance1895333929533392Humanname
405692611CV3315296single nucleotide variantNM_006788.4(RALBP1):c.1744G>A (p.Glu582Lys)not specified [RCV004445626]uncertain significance1895357139535713Humanname
405692615CV3315297single nucleotide variantNM_006788.4(RALBP1):c.1813G>T (p.Ala605Ser)not specified [RCV004445627]uncertain significance1895357829535782Humanname
405692620CV3315298single nucleotide variantNM_006788.4(RALBP1):c.1874T>A (p.Val625Asp)not specified [RCV004445628]uncertain significance1895358439535843Humanname
405692625CV3315299single nucleotide variantNM_006788.4(RALBP1):c.1891G>T (p.Ala631Ser)not specified [RCV004445629]uncertain significance1895358609535860Humanname
407500302CV3472176single nucleotide variantNM_006788.4(RALBP1):c.1840C>T (p.Arg614Cys)not specified [RCV004669524]uncertain significance1895358099535809Humanname
597703888CV3582560single nucleotide variantNM_006788.4(RALBP1):c.1763G>A (p.Arg588His)not specified [RCV004860240]uncertain significance1895357329535732Humanname
597703917CV3582564single nucleotide variantNM_006788.4(RALBP1):c.1381A>T (p.Ser461Cys)not specified [RCV004860243]uncertain significance1895308679530867Humanname
597754005CV3582568single nucleotide variantNM_006788.4(RALBP1):c.1187C>A (p.Ala396Glu)not specified [RCV004847116]likely benign1895247279524727Humanname
598174626CV3905201single nucleotide variantNM_006788.4(RALBP1):c.1741C>T (p.Arg581Cys)not specified [RCV005263885]uncertain significance1895357109535710Humanname
598174634CV3905202single nucleotide variantNM_006788.4(RALBP1):c.1934C>T (p.Ser645Leu)not specified [RCV005263886]uncertain significance1895359039535903Humanname
598174641CV3905203single nucleotide variantNM_006788.4(RALBP1):c.1546C>T (p.Arg516Cys)not specified [RCV005263887]uncertain significance1895334259533425Humanname
598174657CV3905205single nucleotide variantNM_006788.4(RALBP1):c.1742G>A (p.Arg581His)not specified [RCV005263889]uncertain significance1895357119535711Humanname