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


12 records found for search term Wnt8b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598275537CV3937208single nucleotide variantNM_003393.4(WNT8B):c.71C>T (p.Ser24Leu)not specified [RCV005304671]uncertain significance10100479054100479054Humanname
15129116CV712114single nucleotide variantNM_003393.4(WNT8B):c.513G>A (p.Ala171=)not provided [RCV000964204]benign10100482273100482273Humanname
156045080CV2340153single nucleotide variantNM_003393.4(WNT8B):c.248G>A (p.Arg83Gln)not specified [RCV004192390]uncertain significance10100481004100481004Humanname
155914608CV2264559single nucleotide variantNM_003393.4(WNT8B):c.352C>T (p.Arg118Cys)not specified [RCV004132573]uncertain significance10100481108100481108Humanname
155904857CV2298880single nucleotide variantNM_003393.4(WNT8B):c.371G>T (p.Gly124Val)not specified [RCV004156420]uncertain significance10100481915100481915Humanname
156352474CV2323979single nucleotide variantNM_003393.4(WNT8B):c.916G>T (p.Val306Leu)not specified [RCV004176498]uncertain significance10100482676100482676Humanname
405812203CV3352966single nucleotide variantNM_003393.4(WNT8B):c.804A>C (p.Glu268Asp)not specified [RCV004483166]uncertain significance10100482564100482564Humanname
405812205CV3352967single nucleotide variantNM_003393.4(WNT8B):c.928A>G (p.Asn310Asp)not specified [RCV004483167]uncertain significance10100482688100482688Humanname
407524869CV3488001single nucleotide variantNM_003393.4(WNT8B):c.890C>T (p.Ala297Val)not specified [RCV004678588]uncertain significance10100482650100482650Humanname
597741052CV3624264single nucleotide variantNM_003393.4(WNT8B):c.733G>A (p.Glu245Lys)not specified [RCV004890675]uncertain significance10100482493100482493Humanname
597800110CV3624265single nucleotide variantNM_003393.4(WNT8B):c.670G>C (p.Ala224Pro)not specified [RCV004879997]uncertain significance10100482430100482430Humanname
15129120CV712115single nucleotide variantNM_003393.4(WNT8B):c.1002C>A (p.Ser334Arg)not provided [RCV000964205]benign10100482762100482762Humanname