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Variants search result for Homo sapiens
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41 records found for search term Rxrb
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405280526CV3195577single nucleotide variantNM_021976.5(RXRB):c.641-6C>GRXRB-related disorder [RCV003906821]benign63319794733197947Humanname , trait , alternate_id
405273821CV3210521single nucleotide variantNM_001291989.2(RXRB):c.16+9A>CRXRB-related disorder [RCV003917378]likely benign63320075833200758Humanname , trait , alternate_id
155966726CV2329831single nucleotide variantNM_021976.5(RXRB):c.26T>C (p.Phe9Ser)not specified [RCV004183292]uncertain significance63320045133200451Humanname
15110332CV779172duplicationNM_021976.5(RXRB):c.1455-10_1455-5dupRXRB-related disorder [RCV003916033]|not provided [RCV000960878]benign63319483333194834Humanname , trait , alternate_id
405258261CV3203180single nucleotide variantNM_021976.5(RXRB):c.624C>T (p.Cys208=)RXRB-related disorder [RCV003941788]benign63319832433198324Humanname , trait , alternate_id
405701436CV3310074single nucleotide variantNM_021976.5(RXRB):c.53A>G (p.Gln18Arg)not specified [RCV004447152]uncertain significance63320042433200424Humanname
597734175CV3597719single nucleotide variantNM_021976.5(RXRB):c.74G>A (p.Arg25Gln)not specified [RCV004863434]uncertain significance63320040333200403Humanname
150481971CV1244196single nucleotide variantNM_021976.5(RXRB):c.1152C>T (p.Phe384=)RXRB-related disorder [RCV003975833]|not provided [RCV001653042]benign63319567433195674Humanname , trait , alternate_id
401740662CV2702581single nucleotide variantNM_021976.5(RXRB):c.190G>C (p.Glu64Gln)not specified [RCV004317065]uncertain significance63320028733200287Humanname
405285489CV3212574single nucleotide variantNM_021976.5(RXRB):c.1206C>T (p.His402=)RXRB-related disorder [RCV003959145]likely benign63319562033195620Humanname , trait , alternate_id
405293610CV3214306single nucleotide variantNM_021976.5(RXRB):c.1419C>G (p.Thr473=)RXRB-related disorder [RCV003932005]likely benign63319498033194980Humanname , trait , alternate_id
405261942CV3216459single nucleotide variantNM_021976.5(RXRB):c.1194C>T (p.Ala398=)RXRB-related disorder [RCV003944636]likely benign63319563233195632Humanname , trait , alternate_id
405701412CV3310070single nucleotide variantNM_021976.5(RXRB):c.155C>G (p.Ala52Gly)not specified [RCV004447148]uncertain significance63320032233200322Humanname
405701421CV3310071single nucleotide variantNM_021976.5(RXRB):c.196G>C (p.Gly66Arg)not specified [RCV004447149]uncertain significance63320028133200281Humanname
405701425CV3310072single nucleotide variantNM_021976.5(RXRB):c.262C>T (p.Pro88Ser)not specified [RCV004447150]uncertain significance63319939033199390Humanname
156307342CV2252839single nucleotide variantNM_021976.5(RXRB):c.562G>A (p.Gly188Ser)not specified [RCV004120451]uncertain significance63319838633198386Humanname
156066056CV2284459single nucleotide variantNM_021976.5(RXRB):c.874G>C (p.Ala292Pro)not specified [RCV004140650]uncertain significance63319655333196553Humanname
156156098CV2359804single nucleotide variantNM_021976.5(RXRB):c.473G>A (p.Ser158Asn)not specified [RCV004212664]uncertain significance63319917933199179Humanname
329360231CV2458633single nucleotide variantNM_021976.5(RXRB):c.382C>A (p.Pro128Thr)not specified [RCV004268306]uncertain significance63319927033199270Humanname
401726925CV2674603single nucleotide variantNM_021976.5(RXRB):c.971G>A (p.Gly324Glu)not specified [RCV004291473]uncertain significance63319645633196456Humanname
401736593CV2688829single nucleotide variantNM_021976.5(RXRB):c.307C>T (p.Pro103Ser)not specified [RCV004303847]uncertain significance63319934533199345Humanname
401745736CV2693339single nucleotide variantNM_021976.5(RXRB):c.955G>A (p.Val319Ile)not specified [RCV004295302]likely benign63319647233196472Humanname
401781793CV2722276single nucleotide variantNM_021976.5(RXRB):c.382C>G (p.Pro128Ala)not specified [RCV004328831]uncertain significance63319927033199270Humanname
401889919CV2763542single nucleotide variantNM_021976.5(RXRB):c.425C>T (p.Ser142Phe)not specified [RCV004343063]uncertain significance63319922733199227Humanname
405289261CV3218183single nucleotide variantNM_021976.5(RXRB):c.310C>T (p.Pro104Ser)RXRB-related disorder [RCV003983585]likely benign63319934233199342Humanname , trait , alternate_id
405701430CV3310073single nucleotide variantNM_021976.5(RXRB):c.367C>A (p.Pro123Thr)not specified [RCV004447151]uncertain significance63319928533199285Humanname
407468781CV3473258single nucleotide variantNM_021976.5(RXRB):c.973A>G (p.Thr325Ala)not specified [RCV004661234]uncertain significance63319645433196454Humanname
597734152CV3597715single nucleotide variantNM_021976.5(RXRB):c.724C>T (p.Arg242Trp)not specified [RCV004863430]uncertain significance63319785833197858Humanname
597734164CV3597717single nucleotide variantNM_021976.5(RXRB):c.626G>C (p.Gly209Ala)not specified [RCV004863432]uncertain significance63319832233198322Humanname
597734170CV3597718single nucleotide variantNM_021976.5(RXRB):c.503T>A (p.Leu168His)not specified [RCV004863433]uncertain significance63319844533198445Humanname
598234163CV3910129single nucleotide variantNM_021976.5(RXRB):c.887C>A (p.Pro296His)not specified [RCV005274993]uncertain significance63319654033196540Humanname
598234170CV3910130single nucleotide variantNM_021976.5(RXRB):c.864T>G (p.Asp288Glu)not specified [RCV005274994]uncertain significance63319656333196563Humanname
598234177CV3910131single nucleotide variantNM_021976.5(RXRB):c.319C>A (p.Pro107Thr)not specified [RCV005274995]uncertain significance63319933333199333Humanname
156222026CV2343904single nucleotide variantNM_021976.5(RXRB):c.1373G>A (p.Ser458Asn)not specified [RCV004193479]uncertain significance63319502633195026Humanname
405701406CV3310069single nucleotide variantNM_021976.5(RXRB):c.1293G>A (p.Met431Ile)not specified [RCV004447147]uncertain significance63319541833195418Humanname
407514145CV3473257single nucleotide variantNM_021976.5(RXRB):c.1585C>T (p.Pro529Ser)not specified [RCV004674394]uncertain significance63319469933194699Humanname
597734125CV3597710single nucleotide variantNM_021976.5(RXRB):c.1490G>A (p.Arg497Gln)not specified [RCV004863425]uncertain significance63319479433194794Humanname
597734131CV3597711single nucleotide variantNM_021976.5(RXRB):c.1432A>C (p.Lys478Gln)not specified [RCV004863426]uncertain significance63319496733194967Humanname
597734141CV3597713single nucleotide variantNM_021976.5(RXRB):c.1285C>G (p.Arg429Gly)not specified [RCV004863428]uncertain significance63319542633195426Humanname
597734146CV3597714single nucleotide variantNM_021976.5(RXRB):c.1477C>T (p.Leu493Phe)not specified [RCV004863429]uncertain significance63319480733194807Humanname
597734158CV3597716single nucleotide variantNM_021976.5(RXRB):c.1166T>C (p.Ile389Thr)not specified [RCV004863431]uncertain significance63319566033195660Humanname