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Variants search result for Homo sapiens
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22 records found for search term Fam180a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405744149CV3260052single nucleotide variantNM_205855.4(FAM180A):c.57G>C (p.Met19Ile)not specified [RCV004381007]uncertain significance7135748524135748524Humanname
329359334CV2435430single nucleotide variantNM_205855.4(FAM180A):c.101G>A (p.Arg34Gln)not specified [RCV004253082]uncertain significance7135737175135737175Humanname
405744116CV3260047single nucleotide variantNM_205855.4(FAM180A):c.146C>T (p.Thr49Ile)not specified [RCV004381002]uncertain significance7135737130135737130Humanname
407508345CV3435581single nucleotide variantNM_205855.4(FAM180A):c.175G>A (p.Glu59Lys)not specified [RCV004625386]uncertain significance7135737101135737101Humanname
407508352CV3435583single nucleotide variantNM_205855.4(FAM180A):c.112T>A (p.Ser38Thr)not specified [RCV004625388]uncertain significance7135737164135737164Humanname
597738419CV3668748single nucleotide variantNM_205855.4(FAM180A):c.190G>A (p.Glu64Lys)not specified [RCV004921029]uncertain significance7135734307135734307Humanname
156337384CV2228683single nucleotide variantNM_205855.4(FAM180A):c.337A>G (p.Ser113Gly)not specified [RCV004092902]uncertain significance7135734160135734160Humanname
156205010CV2297842single nucleotide variantNM_205855.4(FAM180A):c.467T>C (p.Phe156Ser)not specified [RCV004157786]uncertain significance7135734030135734030Humanname
156260238CV2322285single nucleotide variantNM_205855.4(FAM180A):c.407G>T (p.Arg136Leu)not specified [RCV004176052]uncertain significance7135734090135734090Humanname
156395108CV2325107single nucleotide variantNM_205855.4(FAM180A):c.467T>A (p.Phe156Tyr)not specified [RCV004175636]uncertain significance7135734030135734030Humanname
156273320CV2334006single nucleotide variantNM_205855.4(FAM180A):c.494G>A (p.Arg165His)not specified [RCV004183532]uncertain significance7135734003135734003Humanname
405744120CV3260048single nucleotide variantNM_205855.4(FAM180A):c.357G>C (p.Lys119Asn)not specified [RCV004381003]uncertain significance7135734140135734140Humanname
405744129CV3260049single nucleotide variantNM_205855.4(FAM180A):c.397A>G (p.Thr133Ala)not specified [RCV004381004]likely benign7135734100135734100Humanname
405744138CV3260050single nucleotide variantNM_205855.4(FAM180A):c.484G>A (p.Asp162Asn)not specified [RCV004381005]uncertain significance7135734013135734013Humanname
407508349CV3435582single nucleotide variantNM_205855.4(FAM180A):c.361G>A (p.Glu121Lys)not specified [RCV004625387]uncertain significance7135734136135734136Humanname
597738401CV3668745single nucleotide variantNM_205855.4(FAM180A):c.386C>A (p.Thr129Asn)not specified [RCV004921026]uncertain significance7135734111135734111Humanname
597738408CV3668746single nucleotide variantNM_205855.4(FAM180A):c.313C>T (p.Arg105Cys)not specified [RCV004921027]uncertain significance7135734184135734184Humanname
597738413CV3668747single nucleotide variantNM_205855.4(FAM180A):c.457G>C (p.Val153Leu)not specified [RCV004921028]likely benign7135734040135734040Humanname
597738425CV3668749single nucleotide variantNM_205855.4(FAM180A):c.403T>C (p.Tyr135His)not specified [RCV004921030]uncertain significance7135734094135734094Humanname
597738435CV3668751single nucleotide variantNM_205855.4(FAM180A):c.314G>A (p.Arg105His)not specified [RCV004921032]uncertain significance7135734183135734183Humanname
597738439CV3668752single nucleotide variantNM_205855.4(FAM180A):c.479G>A (p.Arg160Lys)not specified [RCV004921033]uncertain significance7135734018135734018Humanname
598225575CV3962076single nucleotide variantNM_205855.4(FAM180A):c.493C>T (p.Arg165Cys)not specified [RCV005341475]uncertain significance7135734004135734004Humanname