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41 records found for search term Elk3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15162384CV744942single nucleotide variantNM_005230.4(ELK3):c.1125+7G>Anot provided [RCV000903541]benign129625986096259860Humanname
8582484CV117034single nucleotide variantNM_005230.3(ELK3):c.-3+3418A>GLung cancer [RCV000097555]uncertain significance129619812396198123Humanname
155906825CV2303387single nucleotide variantNM_005230.4(ELK3):c.11C>T (p.Ala4Val)not specified [RCV004159118]uncertain significance129622357796223577Humanname
15102648CV702557single nucleotide variantNM_005230.4(ELK3):c.834G>A (p.Ser278=)not provided [RCV000959327]benign129624756696247566Humanname
156095392CV2398947single nucleotide variantNM_005230.4(ELK3):c.270C>G (p.Ile90Met)not specified [RCV004245259]uncertain significance129624700296247002Humanname
15108386CV713799single nucleotide variantNM_005230.4(ELK3):c.1029G>A (p.Pro343=)not provided [RCV000960478]benign129625975796259757Humanname
156186506CV2195675single nucleotide variantNM_005230.4(ELK3):c.602T>C (p.Leu201Pro)not specified [RCV004076038]uncertain significance129624733496247334Humanname
156267186CV2198801single nucleotide variantNM_005230.4(ELK3):c.809C>T (p.Ser270Phe)not specified [RCV004077844]uncertain significance129624754196247541Humanname
156226051CV2215865single nucleotide variantNM_005230.4(ELK3):c.331G>A (p.Asp111Asn)not specified [RCV004096962]uncertain significance129624706396247063Humanname
156308464CV2249515single nucleotide variantNM_005230.4(ELK3):c.922G>A (p.Gly308Ser)not specified [RCV004120549]uncertain significance129624765496247654Humanname
156144976CV2292364single nucleotide variantNM_005230.4(ELK3):c.667T>G (p.Ser223Ala)not specified [RCV004150172]uncertain significance129624739996247399Humanname
329391761CV2445013single nucleotide variantNM_005230.4(ELK3):c.994A>G (p.Thr332Ala)not specified [RCV004261628]uncertain significance129624772696247726Humanname
401899291CV2783819single nucleotide variantNM_005230.4(ELK3):c.652G>C (p.Val218Leu)not specified [RCV004360726]uncertain significance129624738496247384Humanname
405738562CV3238929single nucleotide variantNM_005230.4(ELK3):c.305G>A (p.Arg102Gln)not specified [RCV004380198]uncertain significance129624703796247037Humanname
405738568CV3238930single nucleotide variantNM_005230.4(ELK3):c.347C>T (p.Pro116Leu)not specified [RCV004380199]uncertain significance129624707996247079Humanname
405738577CV3238931single nucleotide variantNM_005230.4(ELK3):c.520C>G (p.Pro174Ala)not specified [RCV004380200]uncertain significance129624725296247252Humanname
405738582CV3238932single nucleotide variantNM_005230.4(ELK3):c.520C>T (p.Pro174Ser)not specified [RCV004380201]uncertain significance129624725296247252Humanname
405738588CV3238933single nucleotide variantNM_005230.4(ELK3):c.608C>T (p.Ser203Phe)not specified [RCV004380202]uncertain significance129624734096247340Humanname
405738595CV3238934single nucleotide variantNM_005230.4(ELK3):c.908C>T (p.Pro303Leu)not specified [RCV004380203]uncertain significance129624764096247640Humanname
405738600CV3238935single nucleotide variantNM_005230.4(ELK3):c.926C>T (p.Thr309Ile)not specified [RCV004380204]uncertain significance129624765896247658Humanname
407506599CV3438277single nucleotide variantNM_005230.4(ELK3):c.664A>G (p.Ile222Val)not specified [RCV004624747]uncertain significance129624739696247396Humanname
407506602CV3438278single nucleotide variantNM_005230.4(ELK3):c.328A>G (p.Ser110Gly)not specified [RCV004624748]uncertain significance129624706096247060Humanname
407506609CV3438280single nucleotide variantNM_005230.4(ELK3):c.772A>G (p.Ser258Gly)not specified [RCV004624750]uncertain significance129624750496247504Humanname
597666227CV3670917single nucleotide variantNM_005230.4(ELK3):c.770G>C (p.Arg257Thr)not specified [RCV004912524]uncertain significance129624750296247502Humanname
597666235CV3670918single nucleotide variantNM_005230.4(ELK3):c.373G>C (p.Gly125Arg)not specified [RCV004912525]uncertain significance129624710596247105Humanname
597746915CV3670919single nucleotide variantNM_005230.4(ELK3):c.997G>A (p.Ala333Thr)not specified [RCV004922795]uncertain significance129624772996247729Humanname
597666244CV3670920single nucleotide variantNM_005230.4(ELK3):c.791C>T (p.Ala264Val)not specified [RCV004912526]uncertain significance129624752396247523Humanname
597666251CV3670921single nucleotide variantNM_005230.4(ELK3):c.865C>G (p.Pro289Ala)not specified [RCV004912527]uncertain significance129624759796247597Humanname
597746920CV3670922single nucleotide variantNM_005230.4(ELK3):c.550A>G (p.Arg184Gly)not specified [RCV004922796]uncertain significance129624728296247282Humanname
597666261CV3670923single nucleotide variantNM_005230.4(ELK3):c.488C>T (p.Thr163Met)not specified [RCV004912528]uncertain significance129624722096247220Humanname
597666269CV3670924single nucleotide variantNM_005230.4(ELK3):c.601C>G (p.Leu201Val)not specified [RCV004912529]uncertain significance129624733396247333Humanname
598190772CV3957724single nucleotide variantNM_005230.4(ELK3):c.305G>T (p.Arg102Leu)not specified [RCV005334743]uncertain significance129624703796247037Humanname
598190786CV3957726single nucleotide variantNM_005230.4(ELK3):c.854C>T (p.Pro285Leu)not specified [RCV005334745]uncertain significance129624758696247586Humanname
598190792CV3957727single nucleotide variantNM_005230.4(ELK3):c.604C>T (p.Pro202Ser)not specified [RCV005334746]uncertain significance129624733696247336Humanname
15185431CV702556single nucleotide variantNM_005230.4(ELK3):c.611C>T (p.Thr204Met)not provided [RCV000952982]likely benign129624734396247343Humanname
15158017CV725322single nucleotide variantNM_005230.4(ELK3):c.678G>A (p.Met226Ile)not provided [RCV000880928]likely benign129624741096247410Humanname
156220928CV2397362single nucleotide variantNM_005230.4(ELK3):c.1149C>A (p.His383Gln)not specified [RCV004238886]uncertain significance129626710596267105Humanname
329360066CV2446549single nucleotide variantNM_005230.4(ELK3):c.1143T>G (p.Asn381Lys)not specified [RCV004251446]uncertain significance129626709996267099Humanname
405738540CV3238926single nucleotide variantNM_005230.4(ELK3):c.1093G>A (p.Ala365Thr)not specified [RCV004380195]uncertain significance129625982196259821Humanname
405738547CV3238927single nucleotide variantNM_005230.4(ELK3):c.1115C>T (p.Thr372Met)not specified [RCV004380196]uncertain significance129625984396259843Humanname
405738553CV3238928single nucleotide variantNM_005230.4(ELK3):c.1190C>T (p.Pro397Leu)not specified [RCV004380197]uncertain significance129626714696267146Humanname