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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


18 records found for search term Dnajc8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401725433CV2721770single nucleotide variantNM_014280.3(DNAJC8):c.25A>T (p.Thr9Ser)not specified [RCV004324504]uncertain significance12823297428232974Humanname
405747696CV3240867single nucleotide variantNM_014280.3(DNAJC8):c.21C>A (p.Ser7Arg)not specified [RCV004381470]uncertain significance12823297828232978Humanname
405747700CV3240868single nucleotide variantNM_014280.3(DNAJC8):c.22G>C (p.Gly8Arg)not specified [RCV004381471]uncertain significance12823297728232977Humanname
598163985CV3953586single nucleotide variantNM_014280.3(DNAJC8):c.14G>C (p.Gly5Ala)not specified [RCV005329453]uncertain significance12823298528232985Humanname
401743293CV2674625single nucleotide variantNM_014280.3(DNAJC8):c.47C>T (p.Thr16Ile)not specified [RCV004293925]uncertain significance12823295228232952Humanname
405747715CV3240870single nucleotide variantNM_014280.3(DNAJC8):c.32G>A (p.Gly11Asp)not specified [RCV004381473]uncertain significance12823296728232967Humanname
598163990CV3953587single nucleotide variantNM_014280.3(DNAJC8):c.29C>T (p.Ser10Leu)not specified [RCV005329454]uncertain significance12823297028232970Humanname
598164002CV3953589single nucleotide variantNM_014280.3(DNAJC8):c.43A>G (p.Ser15Gly)not specified [RCV005329456]uncertain significance12823295628232956Humanname
329401727CV2457340single nucleotide variantNM_014280.3(DNAJC8):c.164A>G (p.Asn55Ser)not specified [RCV004267180]uncertain significance12822893828228938Humanname
405747710CV3240869single nucleotide variantNM_014280.3(DNAJC8):c.278C>T (p.Ala93Val)not specified [RCV004381472]uncertain significance12821059728210597Humanname
597644565CV3663048single nucleotide variantNM_014280.3(DNAJC8):c.145C>G (p.Pro49Ala)not specified [RCV004909620]uncertain significance12822895728228957Humanname
598163967CV3953583single nucleotide variantNM_014280.3(DNAJC8):c.199G>A (p.Glu67Lys)not specified [RCV005329450]uncertain significance12821497828214978Humanname
598163995CV3953588single nucleotide variantNM_014280.3(DNAJC8):c.283A>G (p.Arg95Gly)not specified [RCV005329455]uncertain significance12821059228210592Humanname
405747733CV3240872single nucleotide variantNM_014280.3(DNAJC8):c.537G>C (p.Glu179Asp)not specified [RCV004381475]uncertain significance12820528428205284Humanname
405747740CV3240873single nucleotide variantNM_014280.3(DNAJC8):c.689C>G (p.Thr230Arg)not specified [RCV004381476]uncertain significance12820132128201321Humanname
597714102CV3663047single nucleotide variantNM_014280.3(DNAJC8):c.653G>A (p.Gly218Asp)not specified [RCV004918094]uncertain significance12820135728201357Humanname
597714113CV3663049single nucleotide variantNM_014280.3(DNAJC8):c.438A>C (p.Lys146Asn)not specified [RCV004918095]uncertain significance12820837528208375Humanname
598163973CV3953584single nucleotide variantNM_014280.3(DNAJC8):c.481G>A (p.Ala161Thr)not specified [RCV005329451]uncertain significance12820534028205340Humanname