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


15 records found for search term Jazf1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150454710CV1277053single nucleotide variantNM_175061.4(JAZF1):c.115+30671A>Gnot provided [RCV001708844]benign72814979228149792Humanname
617153047CV4021021single nucleotide variantNM_175061.4(JAZF1):c.702G>A (p.Ser234=)not provided [RCV005428774]likely benign72783283027832830Humanname
156277317CV2255889single nucleotide variantNM_175061.4(JAZF1):c.117T>A (p.Asp39Glu)not specified [RCV004122042]uncertain significance72799198027991980Humanname
156090371CV2299957single nucleotide variantNM_175061.4(JAZF1):c.128G>A (p.Arg43Gln)not specified [RCV004151175]uncertain significance72799196927991969Humanname
156224070CV2395076single nucleotide variantNM_175061.4(JAZF1):c.251T>C (p.Leu84Pro)not specified [RCV004236760]uncertain significance72789535427895354Humanname
598211998CV3969356single nucleotide variantNM_175061.4(JAZF1):c.208C>T (p.Arg70Cys)not specified [RCV005358768]uncertain significance72789539727895397Humanname
598172494CV3969357single nucleotide variantNM_175061.4(JAZF1):c.194T>C (p.Met65Thr)not specified [RCV005370784]uncertain significance72789541127895411Humanname
329353281CV2469089single nucleotide variantNM_175061.4(JAZF1):c.695C>T (p.Pro232Leu)not specified [RCV004274326]uncertain significance72783283727832837Humanname
401744411CV2696995single nucleotide variantNM_175061.4(JAZF1):c.312C>A (p.Ser104Arg)not specified [RCV004292987]uncertain significance72789529327895293Humanname
401861131CV2769530single nucleotide variantNM_175061.4(JAZF1):c.488T>C (p.Met163Thr)not specified [RCV004351187]uncertain significance72784076527840765Humanname
405795255CV3275384single nucleotide variantNM_175061.4(JAZF1):c.433G>A (p.Asp145Asn)not specified [RCV004401158]uncertain significance72784082027840820Humanname
597777333CV3691251single nucleotide variantNM_175061.4(JAZF1):c.320G>A (p.Ser107Asn)not specified [RCV004929846]uncertain significance72789528527895285Humanname
597777337CV3691252single nucleotide variantNM_175061.4(JAZF1):c.608G>A (p.Arg203His)not specified [RCV004929847]uncertain significance72783292427832924Humanname
597777341CV3691253single nucleotide variantNM_175061.4(JAZF1):c.691C>A (p.Pro231Thr)not specified [RCV004929848]uncertain significance72783284127832841Humanname
598258684CV3969355single nucleotide variantNM_175061.4(JAZF1):c.503G>A (p.Gly168Glu)not specified [RCV005347257]uncertain significance72784075027840750Humanname