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Variants search result for Homo sapiens
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20 records found for search term Kpna1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8577969CV112346single nucleotide variantNM_002264.3(KPNA1):c.996+1700C>GLung cancer [RCV000092869]uncertain significance3122440338122440338Humanname
405817042CV3272788single nucleotide variantNM_002264.4(KPNA1):c.92A>G (p.Glu31Gly)not specified [RCV004412033]uncertain significance3122496474122496474Humanname
156124078CV2234182single nucleotide variantNM_002264.4(KPNA1):c.224T>C (p.Met75Thr)not specified [RCV004106268]uncertain significance3122467335122467335Humanname
401856892CV2755164single nucleotide variantNM_002264.4(KPNA1):c.271A>T (p.Ile91Leu)not specified [RCV004335312]uncertain significance3122464008122464008Humanname
405817089CV3272786single nucleotide variantNM_002264.4(KPNA1):c.155C>T (p.Thr52Ile)not specified [RCV004412031]uncertain significance3122467404122467404Humanname
598183703CV3984083single nucleotide variantNM_002264.4(KPNA1):c.186G>A (p.Met62Ile)not specified [RCV005352946]uncertain significance3122467373122467373Humanname
15191855CV697778single nucleotide variantNM_002264.4(KPNA1):c.1185G>A (p.Arg395=)not provided [RCV000954898]benign3122433726122433726Humanname
155908500CV2354653single nucleotide variantNM_002264.4(KPNA1):c.636C>G (p.Ile212Met)not specified [RCV004202617]uncertain significance3122451993122451993Humanname
329396772CV2459087single nucleotide variantNM_002264.4(KPNA1):c.889G>A (p.Val297Ile)not specified [RCV004272550]uncertain significance3122449602122449602Humanname
401782980CV2707649single nucleotide variantNM_002264.4(KPNA1):c.772G>T (p.Val258Leu)not specified [RCV004306585]uncertain significance3122449719122449719Humanname
405817065CV3272787single nucleotide variantNM_002264.4(KPNA1):c.517A>G (p.Ile173Val)not specified [RCV004412032]uncertain significance3122453917122453917Humanname
598221743CV3984081single nucleotide variantNM_002264.4(KPNA1):c.749C>T (p.Ala250Val)not specified [RCV005360854]uncertain significance3122451538122451538Humanname
598162427CV3984082single nucleotide variantNM_002264.4(KPNA1):c.640C>T (p.Pro214Ser)not specified [RCV005368636]uncertain significance3122451989122451989Humanname
155960514CV2252859single nucleotide variantNM_002264.4(KPNA1):c.1258G>A (p.Val420Ile)not specified [RCV004120468]uncertain significance3122427709122427709Humanname
156188503CV2328629single nucleotide variantNM_002264.4(KPNA1):c.1426T>G (p.Tyr476Asp)not specified [RCV004177881]uncertain significance3122427541122427541Humanname
155933654CV2399362single nucleotide variantNM_002264.4(KPNA1):c.1537A>G (p.Ile513Val)not specified [RCV004242650]uncertain significance3122427065122427065Humanname
405817122CV3272785single nucleotide variantNM_002264.4(KPNA1):c.1022A>G (p.Gln341Arg)not specified [RCV004412030]uncertain significance3122437270122437270Humanname
407499487CV3448838single nucleotide variantNM_002264.4(KPNA1):c.1160G>A (p.Ser387Asn)not specified [RCV004644340]uncertain significance3122433751122433751Humanname
597797598CV3698193single nucleotide variantNM_002264.4(KPNA1):c.1072G>A (p.Ala358Thr)not specified [RCV004935859]uncertain significance3122437220122437220Humanname
598162421CV3984080single nucleotide variantNM_002264.4(KPNA1):c.1532G>T (p.Ser511Ile)not specified [RCV005368635]uncertain significance3122427070122427070Humanname