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Variants search result for Homo sapiens
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27 records found for search term Rell2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329398542CV2471598single nucleotide variantNM_173828.5(RELL2):c.19G>A (p.Asp7Asn)not specified [RCV004286895]uncertain significance5141638244141638244Humanname
156300426CV2322457single nucleotide variantNM_173828.5(RELL2):c.217G>A (p.Glu73Lys)not specified [RCV004180579]uncertain significance5141638827141638827Humanname
156071323CV2353138single nucleotide variantNM_173828.5(RELL2):c.160C>T (p.Pro54Ser)not specified [RCV004203616]uncertain significance5141638385141638385Humanname
329388374CV2466311single nucleotide variantNM_173828.5(RELL2):c.190G>C (p.Asp64His)not specified [RCV004280236]uncertain significance5141638800141638800Humanname
405683463CV3315702single nucleotide variantNM_173828.5(RELL2):c.230G>A (p.Arg77His)not specified [RCV004443859]uncertain significance5141638840141638840Humanname
407458931CV3465310single nucleotide variantNM_173828.5(RELL2):c.209A>G (p.Asp70Gly)not specified [RCV004658088]uncertain significance5141638819141638819Humanname
156062498CV2277213single nucleotide variantNM_173828.5(RELL2):c.434G>A (p.Arg145His)not specified [RCV004142841]uncertain significance5141639580141639580Humanname
155906008CV2303226single nucleotide variantNM_173828.5(RELL2):c.334A>G (p.Ser112Gly)not specified [RCV004156982]uncertain significance5141639480141639480Humanname
156270699CV2312230single nucleotide variantNM_173828.5(RELL2):c.691G>A (p.Val231Ile)not specified [RCV004165121]uncertain significance5141640107141640107Humanname
156065798CV2348908single nucleotide variantNM_173828.5(RELL2):c.730G>A (p.Asp244Asn)not specified [RCV004203343]uncertain significance5141640146141640146Humanname
156347341CV2349581single nucleotide variantNM_173828.5(RELL2):c.589G>T (p.Gly197Trp)not specified [RCV004204007]uncertain significance5141640005141640005Humanname
329374077CV2434690single nucleotide variantNM_173828.5(RELL2):c.775T>C (p.Ser259Pro)not specified [RCV004248406]uncertain significance5141640191141640191Humanname
401746569CV2678870single nucleotide variantNM_173828.5(RELL2):c.450G>T (p.Lys150Asn)not specified [RCV004292848]uncertain significance5141639596141639596Humanname
401878624CV2754720single nucleotide variantNM_173828.5(RELL2):c.671C>A (p.Pro224His)not specified [RCV004339388]uncertain significance5141640087141640087Humanname
405683466CV3315703single nucleotide variantNM_173828.5(RELL2):c.386C>T (p.Ala129Val)not specified [RCV004443860]uncertain significance5141639532141639532Humanname
405683470CV3315704single nucleotide variantNM_173828.5(RELL2):c.604G>A (p.Gly202Arg)not specified [RCV004443861]uncertain significance5141640020141640020Humanname
407487051CV3465306single nucleotide variantNM_173828.5(RELL2):c.896G>A (p.Gly299Glu)not specified [RCV004671800]uncertain significance5141640428141640428Humanname
407487057CV3465307single nucleotide variantNM_173828.5(RELL2):c.425C>T (p.Pro142Leu)not specified [RCV004671801]uncertain significance5141639571141639571Humanname
407487065CV3465309single nucleotide variantNM_173828.5(RELL2):c.802G>A (p.Gly268Arg)not specified [RCV004671802]uncertain significance5141640218141640218Humanname
597730824CV3593219single nucleotide variantNM_173828.5(RELL2):c.664C>A (p.Leu222Met)not specified [RCV004863069]uncertain significance5141640080141640080Humanname
597765125CV3593220single nucleotide variantNM_173828.5(RELL2):c.442C>T (p.Arg148Cys)not specified [RCV004849953]uncertain significance5141639588141639588Humanname
597730835CV3593221single nucleotide variantNM_173828.5(RELL2):c.648G>C (p.Met216Ile)not specified [RCV004863070]uncertain significance5141640064141640064Humanname
597730845CV3593222single nucleotide variantNM_173828.5(RELL2):c.749G>A (p.Arg250His)not specified [RCV004863071]uncertain significance5141640165141640165Humanname
597730853CV3593223single nucleotide variantNM_173828.5(RELL2):c.734G>C (p.Ser245Thr)not specified [RCV004863072]uncertain significance5141640150141640150Humanname
597765129CV3593224single nucleotide variantNM_173828.5(RELL2):c.521T>C (p.Ile174Thr)not specified [RCV004849954]uncertain significance5141639937141639937Humanname
597765131CV3593225single nucleotide variantNM_173828.5(RELL2):c.299G>C (p.Gly100Ala)not specified [RCV004849955]uncertain significance5141639003141639003Humanname
598204342CV3909317single nucleotide variantNM_173828.5(RELL2):c.677G>C (p.Arg226Thr)not specified [RCV005269525]uncertain significance5141640093141640093Humanname