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Variants search result for Homo sapiens
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20 records found for search term Ubxn8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156279147CV2316734single nucleotide variantNM_005671.4(UBXN8):c.68G>A (p.Arg23Gln)not specified [RCV004171957]uncertain significance83074425730744257Humanname
407523472CV3491232single nucleotide variantNM_005671.4(UBXN8):c.53T>C (p.Val18Ala)not specified [RCV004677953]uncertain significance83074424230744242Humanname
156109255CV2254530single nucleotide variantNM_005671.4(UBXN8):c.182C>T (p.Ser61Leu)not specified [RCV004123888]uncertain significance83075148930751489Humanname
155953714CV2303116single nucleotide variantNM_005671.4(UBXN8):c.196C>G (p.Gln66Glu)not specified [RCV004156892]uncertain significance83075150330751503Humanname
329400146CV2440671single nucleotide variantNM_005671.4(UBXN8):c.119G>A (p.Arg40Gln)not specified [RCV004256579]uncertain significance83075142630751426Humanname
329398937CV2471800single nucleotide variantNM_005671.4(UBXN8):c.199G>A (p.Val67Ile)not specified [RCV004280839]uncertain significance83075150630751506Humanname
155995912CV2250400single nucleotide variantNM_005671.4(UBXN8):c.407G>T (p.Gly136Val)not specified [RCV004127280]uncertain significance83075676630756766Humanname
155904653CV2385563single nucleotide variantNM_005671.4(UBXN8):c.484T>G (p.Leu162Val)not specified [RCV004233202]likely benign83075684330756843Humanname
156320037CV2400249single nucleotide variantNM_005671.4(UBXN8):c.497C>T (p.Pro166Leu)not specified [RCV004243041]uncertain significance83075685630756856Humanname
401743730CV2688016single nucleotide variantNM_005671.4(UBXN8):c.365C>T (p.Thr122Met)not specified [RCV004305090]uncertain significance83075474730754747Humanname
401730297CV2711185single nucleotide variantNM_005671.4(UBXN8):c.368G>A (p.Gly123Asp)not specified [RCV004312984]uncertain significance83075475030754750Humanname
401741136CV2713389single nucleotide variantNM_005671.4(UBXN8):c.550C>T (p.Pro184Ser)not specified [RCV004319012]uncertain significance83076090930760909Humanname
405800424CV3337875single nucleotide variantNM_005671.4(UBXN8):c.314C>T (p.Pro105Leu)not specified [RCV004477262]uncertain significance83075469630754696Humanname
405800426CV3337876single nucleotide variantNM_005671.4(UBXN8):c.422G>A (p.Ser141Asn)not specified [RCV004477263]uncertain significance83075678130756781Humanname
405800427CV3337877single nucleotide variantNM_005671.4(UBXN8):c.619A>G (p.Arg207Gly)not specified [RCV004477264]uncertain significance83076332130763321Humanname
407523469CV3491233single nucleotide variantNM_005671.4(UBXN8):c.532C>G (p.Pro178Ala)not specified [RCV004677954]uncertain significance83076089130760891Humanname
407523466CV3491234single nucleotide variantNM_005671.4(UBXN8):c.606T>A (p.Asn202Lys)not specified [RCV004677955]uncertain significance83076330830763308Humanname
407523463CV3491235single nucleotide variantNM_005671.4(UBXN8):c.602G>C (p.Gly201Ala)not specified [RCV004677956]uncertain significance83076330430763304Humanname
598265904CV3929137single nucleotide variantNM_005671.4(UBXN8):c.412G>A (p.Glu138Lys)not specified [RCV005301819]uncertain significance83075677130756771Humanname
598265910CV3929138single nucleotide variantNM_005671.4(UBXN8):c.536A>G (p.Asp179Gly)not specified [RCV005301820]uncertain significance83076089530760895Humanname