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Variants search result for Homo sapiens
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25 records found for search term Cbll1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597760769CV3641239single nucleotide variantNM_024814.4(CBLL1):c.4G>A (p.Asp2Asn)not specified [RCV004894795]uncertain significance7107744167107744167Humanname
8632273CV87481single nucleotide variantNM_024814.3(CBLL1):c.47C>T (p.Ser16Phe)Malignant melanoma [RCV000067572]not provided7107748913107748913Humanname
401876543CV2761098single nucleotide variantNM_024814.4(CBLL1):c.113C>T (p.Ala38Val)not specified [RCV004338757]uncertain significance7107748979107748979Humanname
405738356CV3292047single nucleotide variantNM_024814.4(CBLL1):c.136A>G (p.Arg46Gly)not specified [RCV004430311]uncertain significance7107749002107749002Humanname
405738363CV3292048single nucleotide variantNM_024814.4(CBLL1):c.173G>A (p.Gly58Asp)not specified [RCV004430312]uncertain significance7107749039107749039Humanname
407482375CV3421970single nucleotide variantNM_024814.4(CBLL1):c.154C>T (p.Pro52Ser)not specified [RCV004602670]uncertain significance7107749020107749020Humanname
597760643CV3641242single nucleotide variantNM_024814.4(CBLL1):c.122C>T (p.Ala41Val)not specified [RCV004894796]uncertain significance7107748988107748988Humanname
156295813CV2239788single nucleotide variantNM_024814.4(CBLL1):c.803C>G (p.Ser268Cys)not specified [RCV004108313]uncertain significance7107758505107758505Humanname
155905820CV2303189single nucleotide variantNM_024814.4(CBLL1):c.409C>T (p.His137Tyr)not specified [RCV004156952]uncertain significance7107755460107755460Humanname
401725327CV2697363single nucleotide variantNM_024814.4(CBLL1):c.782G>A (p.Arg261His)not specified [RCV004304114]uncertain significance7107758484107758484Humanname
405738369CV3292049single nucleotide variantNM_024814.4(CBLL1):c.313C>G (p.Pro105Ala)not specified [RCV004430313]uncertain significance7107753925107753925Humanname
597785662CV3641241single nucleotide variantNM_024814.4(CBLL1):c.884T>C (p.Val295Ala)not specified [RCV004900783]uncertain significance7107758586107758586Humanname
598176083CV3950410single nucleotide variantNM_024814.4(CBLL1):c.644A>C (p.Glu215Ala)not specified [RCV005309971]uncertain significance7107758346107758346Humanname
155917267CV2236515single nucleotide variantNM_024814.4(CBLL1):c.1460G>A (p.Arg487Lys)not specified [RCV004110514]uncertain significance7107759162107759162Humanname
156296368CV2236516single nucleotide variantNM_024814.4(CBLL1):c.1461A>T (p.Arg487Ser)not specified [RCV004110515]uncertain significance7107759163107759163Humanname
156282247CV2348842single nucleotide variantNM_024814.4(CBLL1):c.1223C>T (p.Pro408Leu)not specified [RCV004203285]uncertain significance7107758925107758925Humanname
401893822CV2759857single nucleotide variantNM_024814.4(CBLL1):c.1223C>G (p.Pro408Arg)not specified [RCV004345290]uncertain significance7107758925107758925Humanname
405738349CV3292046single nucleotide variantNM_024814.4(CBLL1):c.1274A>T (p.Asn425Ile)not specified [RCV004430310]uncertain significance7107758976107758976Humanname
407482381CV3421971single nucleotide variantNM_024814.4(CBLL1):c.1250C>G (p.Thr417Ser)not specified [RCV004602671]uncertain significance7107758952107758952Humanname
597785658CV3641240single nucleotide variantNM_024814.4(CBLL1):c.1129A>G (p.Met377Val)not specified [RCV004900782]uncertain significance7107758831107758831Humanname
598176091CV3950411single nucleotide variantNM_024814.4(CBLL1):c.1426C>T (p.Pro476Ser)not specified [RCV005309972]uncertain significance7107759128107759128Humanname
598226942CV3950412single nucleotide variantNM_024814.4(CBLL1):c.1213G>A (p.Gly405Arg)not specified [RCV005318840]uncertain significance7107758915107758915Humanname
598176098CV3950413single nucleotide variantNM_024814.4(CBLL1):c.1256C>A (p.Pro419His)not specified [RCV005309973]uncertain significance7107758958107758958Humanname
598226947CV3950414single nucleotide variantNM_024814.4(CBLL1):c.1163C>T (p.Pro388Leu)not specified [RCV005318841]uncertain significance7107758865107758865Humanname
8626303CV81447single nucleotide variantNM_024814.3(CBLL1):c.1096C>T (p.His366Tyr)Malignant melanoma [RCV000061525]not provided7107758798107758798Humanname