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Variants search result for Homo sapiens
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13 records found for search term Efna2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156384811CV2371606single nucleotide variantNM_001405.4(EFNA2):c.7C>T (p.Pro3Ser)not specified [RCV004216853]uncertain significance1912861751286175Humanname
598167458CV3964875single nucleotide variantNM_001405.4(EFNA2):c.17G>C (p.Arg6Pro)not specified [RCV005330051]uncertain significance1912861851286185Humanname
407497851CV3441765single nucleotide variantNM_001405.4(EFNA2):c.98A>C (p.Asn33Thr)not specified [RCV004622312]uncertain significance1912862661286266Humanname
597736514CV3664330single nucleotide variantNM_001405.4(EFNA2):c.64C>A (p.Pro22Thr)not specified [RCV004920650]uncertain significance1912862321286232Humanname
329369485CV2461129single nucleotide variantNM_001405.4(EFNA2):c.245C>T (p.Pro82Leu)not specified [RCV004265548]uncertain significance1912956491295649Humanname
329395970CV2463121single nucleotide variantNM_001405.4(EFNA2):c.100T>A (p.Ser34Thr)not specified [RCV004274917]uncertain significance1912862681286268Humanname
155963389CV2388391single nucleotide variantNM_001405.4(EFNA2):c.470A>G (p.Asn157Ser)not specified [RCV004234840]uncertain significance1912985661298566Humanname
329393798CV2449865single nucleotide variantNM_001405.4(EFNA2):c.455C>T (p.Ser152Phe)not specified [RCV004268956]uncertain significance1912985511298551Humanname
401767711CV2729852single nucleotide variantNM_001405.4(EFNA2):c.364G>A (p.Gly122Arg)not specified [RCV004332859]uncertain significance1912957681295768Humanname
405715968CV3241663single nucleotide variantNM_001405.4(EFNA2):c.518C>A (p.Thr173Asn)not specified [RCV004377400]uncertain significance1912986141298614Humanname
405715974CV3241664single nucleotide variantNM_001405.4(EFNA2):c.581C>T (p.Pro194Leu)not specified [RCV004377401]likely benign1912998841299884Humanname
407497859CV3441767single nucleotide variantNM_001405.4(EFNA2):c.482G>A (p.Arg161Gln)not specified [RCV004622314]uncertain significance1912985781298578Humanname
598167452CV3964874single nucleotide variantNM_001405.4(EFNA2):c.370C>T (p.Leu124Phe)not specified [RCV005330050]uncertain significance1912957741295774Humanname