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Variants search result for Homo sapiens
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41 records found for search term Rmnd5b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
11592209CV299086single nucleotide variantNM_022762.5(RMND5B):c.*1641T>CDyskeratosis Congenita, Recessive [RCV000336470]uncertain significance5178149673178149673Humanname
405690529CV3227352single nucleotide variantNM_022762.5(RMND5B):c.*1800C>Gnot provided [RCV003991696]uncertain significance5178149832178149832Humanname
405753705CV3316292single nucleotide variantNM_022762.5(RMND5B):c.88G>C (p.Glu30Gln)not specified [RCV004454177]uncertain significance5178138207178138207Humanname
597685803CV3593836single nucleotide variantNM_022762.5(RMND5B):c.79C>T (p.Arg27Trp)not specified [RCV004858312]uncertain significance5178138198178138198Humanname
597754308CV3593839single nucleotide variantNM_022762.5(RMND5B):c.82A>C (p.Ser28Arg)not specified [RCV004847323]uncertain significance5178138201178138201Humanname
598230206CV3899316single nucleotide variantNM_022762.5(RMND5B):c.80G>A (p.Arg27Gln)not specified [RCV005274308]likely benign5178138199178138199Humanname
156219097CV2254013single nucleotide variantNM_022762.5(RMND5B):c.100C>T (p.His34Tyr)not specified [RCV004129469]uncertain significance5178138219178138219Humanname
155958812CV2278368single nucleotide variantNM_022762.5(RMND5B):c.119G>A (p.Arg40Gln)not specified [RCV004132830]uncertain significance5178138238178138238Humanname
401885387CV2762925single nucleotide variantNM_022762.5(RMND5B):c.196C>T (p.Arg66Trp)not specified [RCV004342676]uncertain significance5178142639178142639Humanname
405753678CV3316287single nucleotide variantNM_022762.5(RMND5B):c.152C>A (p.Thr51Asn)not specified [RCV004454172]uncertain significance5178142595178142595Humanname
407508535CV3483423single nucleotide variantNM_022762.5(RMND5B):c.197G>A (p.Arg66Gln)not specified [RCV004672073]uncertain significance5178142640178142640Humanname
597685793CV3593834single nucleotide variantNM_022762.5(RMND5B):c.212C>T (p.Thr71Met)not specified [RCV004858311]uncertain significance5178142655178142655Humanname
597685837CV3593841single nucleotide variantNM_022762.5(RMND5B):c.292G>A (p.Asp98Asn)not specified [RCV004858316]uncertain significance5178142858178142858Humanname
155965702CV2206553single nucleotide variantNM_022762.5(RMND5B):c.406G>A (p.Val136Met)not specified [RCV004080901]uncertain significance5178142972178142972Humanname
156388470CV2231842single nucleotide variantNM_022762.5(RMND5B):c.721G>A (p.Val241Met)not specified [RCV004098644]uncertain significance5178146140178146140Humanname
156192272CV2255354single nucleotide variantNM_022762.5(RMND5B):c.808C>T (p.Arg270Trp)not specified [RCV004117724]uncertain significance5178146227178146227Humanname
156162557CV2323541single nucleotide variantNM_022762.5(RMND5B):c.949A>G (p.Lys317Glu)not specified [RCV004165741]uncertain significance5178147621178147621Humanname
156360689CV2329580single nucleotide variantNM_022762.5(RMND5B):c.308G>A (p.Gly103Asp)not specified [RCV004180705]uncertain significance5178142874178142874Humanname
156061439CV2351325single nucleotide variantNM_022762.5(RMND5B):c.335C>T (p.Ala112Val)not specified [RCV004193029]uncertain significance5178142901178142901Humanname
155908128CV2354571single nucleotide variantNM_022762.5(RMND5B):c.921G>T (p.Gln307His)not specified [RCV004202546]uncertain significance5178147593178147593Humanname
156342859CV2368634single nucleotide variantNM_022762.5(RMND5B):c.962C>T (p.Pro321Leu)not specified [RCV004221410]uncertain significance5178147634178147634Humanname
329379443CV2443413single nucleotide variantNM_022762.5(RMND5B):c.535G>A (p.Val179Ile)not specified [RCV004262255]uncertain significance5178143949178143949Humanname
401734449CV2690591single nucleotide variantNM_022762.5(RMND5B):c.971T>C (p.Ile324Thr)not specified [RCV004304685]uncertain significance5178147736178147736Humanname
401773576CV2709385single nucleotide variantNM_022762.5(RMND5B):c.304T>C (p.Cys102Arg)not specified [RCV004316525]uncertain significance5178142870178142870Humanname
405753684CV3316288single nucleotide variantNM_022762.5(RMND5B):c.370A>G (p.Ile124Val)not specified [RCV004454173]uncertain significance5178142936178142936Humanname
405753689CV3316289single nucleotide variantNM_022762.5(RMND5B):c.776G>A (p.Ser259Asn)not specified [RCV004454174]uncertain significance5178146195178146195Humanname
405753694CV3316290single nucleotide variantNM_022762.5(RMND5B):c.793T>C (p.Cys265Arg)not specified [RCV004454175]uncertain significance5178146212178146212Humanname
405753700CV3316291single nucleotide variantNM_022762.5(RMND5B):c.809G>A (p.Arg270Gln)not specified [RCV004454176]uncertain significance5178146228178146228Humanname
405753711CV3316293single nucleotide variantNM_022762.5(RMND5B):c.943A>G (p.Asn315Asp)not specified [RCV004454178]uncertain significance5178147615178147615Humanname
407475917CV3483424single nucleotide variantNM_022762.5(RMND5B):c.629C>T (p.Ala210Val)not specified [RCV004663345]uncertain significance5178144043178144043Humanname
407475922CV3483425single nucleotide variantNM_022762.5(RMND5B):c.464C>G (p.Pro155Arg)not specified [RCV004663346]uncertain significance5178143664178143664Humanname
597685812CV3593837single nucleotide variantNM_022762.5(RMND5B):c.338G>A (p.Arg113Gln)not specified [RCV004858313]uncertain significance5178142904178142904Humanname
597685821CV3593838single nucleotide variantNM_022762.5(RMND5B):c.550C>T (p.Arg184Cys)not specified [RCV004858314]uncertain significance5178143964178143964Humanname
597685829CV3593840single nucleotide variantNM_022762.5(RMND5B):c.566A>G (p.Asn189Ser)not specified [RCV004858315]uncertain significance5178143980178143980Humanname
597754312CV3593842single nucleotide variantNM_022762.5(RMND5B):c.659G>C (p.Arg220Pro)not specified [RCV004847324]uncertain significance5178144073178144073Humanname
597685845CV3593843single nucleotide variantNM_022762.5(RMND5B):c.670C>T (p.Pro224Ser)not specified [RCV004858317]uncertain significance5178144084178144084Humanname
598230211CV3899317single nucleotide variantNM_022762.5(RMND5B):c.608G>A (p.Arg203His)not specified [RCV005274309]uncertain significance5178144022178144022Humanname
598230217CV3899318single nucleotide variantNM_022762.5(RMND5B):c.965T>C (p.Ile322Thr)not specified [RCV005274310]uncertain significance5178147730178147730Humanname
155971037CV2214052single nucleotide variantNM_022762.5(RMND5B):c.1034C>T (p.Thr345Met)not specified [RCV004084098]uncertain significance5178147799178147799Humanname
405753661CV3316285single nucleotide variantNM_022762.5(RMND5B):c.1043C>G (p.Ser348Cys)not specified [RCV004454170]uncertain significance5178147808178147808Humanname
405753667CV3316286single nucleotide variantNM_022762.5(RMND5B):c.1063A>G (p.Ile355Val)not specified [RCV004454171]uncertain significance5178147828178147828Humanname