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23 records found for search term Ssbp2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8581238CV115675single nucleotide variantNM_001256732.1(SSBP2):c.712-3131A>TLung cancer [RCV000096198]uncertain significance58145195681451956Humanname
8581240CV115677single nucleotide variantNM_001256732.1(SSBP2):c.63-24111C>ALung cancer [RCV000096200]uncertain significance58167445081674450Humanname
8581241CV115678single nucleotide variantNM_001256732.1(SSBP2):c.63-46374G>ALung cancer [RCV000096201]uncertain significance58169671381696713Humanname
8581242CV115679single nucleotide variantNM_001256732.1(SSBP2):c.63-48753A>GLung cancer [RCV000096202]uncertain significance58169909281699092Humanname
8626049CV81193single nucleotide variantNM_012446.3(SSBP2):c.709C>T (p.Pro237Ser)Malignant melanoma [RCV000061271]not provided58144880481448804Humanname
8631725CV86931single nucleotide variantNM_012446.3(SSBP2):c.731C>T (p.Pro244Leu)Malignant melanoma [RCV000067022]not provided58144691581446915Humanname
156079554CV2226552single nucleotide variantNM_001256732.3(SSBP2):c.34G>A (p.Val12Ile)not specified [RCV004101810]uncertain significance58175100981751009Humanname
156140180CV2247008single nucleotide variantNM_001256732.3(SSBP2):c.91C>T (p.Leu31Phe)not specified [RCV004114573]uncertain significance58165031181650311Humanname
12741229CV359714duplicationNM_001256732.3(SSBP2):c.152dup (p.Asn51fs)not specified [RCV000414474]uncertain significance58163660181636602Humanname
156226633CV2352763single nucleotide variantNM_001256732.3(SSBP2):c.112T>G (p.Ser38Ala)not specified [RCV004198780]uncertain significance58165029081650290Humanname
597681256CV3611733single nucleotide variantNM_001256732.3(SSBP2):c.239A>G (p.Glu80Gly)not specified [RCV004857514]uncertain significance58161551681615516Humanname
9686981CV171405single nucleotide variantNM_001256732.3(SSBP2):c.743A>T (p.Tyr248Phe)Prostate cancer [RCV000149200]uncertain significance58144879481448794Human2name
156175739CV2331119single nucleotide variantNM_001256732.3(SSBP2):c.745G>A (p.Val249Ile)not specified [RCV004181732]uncertain significance58144879281448792Humanname
156216458CV2348008single nucleotide variantNM_001256732.3(SSBP2):c.962A>G (p.Asp321Gly)not specified [RCV004197691]uncertain significance58143744981437449Humanname
401762565CV2696167single nucleotide variantNM_001256732.3(SSBP2):c.565C>T (p.Pro189Ser)not specified [RCV004310221]uncertain significance58147370581473705Humanname
401734544CV2709532single nucleotide variantNM_001256732.3(SSBP2):c.991A>G (p.Asn331Asp)not specified [RCV004318769]uncertain significance58142867481428674Humanname
401890542CV2778855single nucleotide variantNM_001256732.3(SSBP2):c.830A>G (p.Tyr277Cys)not specified [RCV004346745]uncertain significance58144269681442696Humanname
405703474CV3326949single nucleotide variantNM_001256732.3(SSBP2):c.674G>A (p.Gly225Asp)not specified [RCV004460731]uncertain significance58146109281461092Humanname
407516892CV3474909single nucleotide variantNM_001256732.3(SSBP2):c.389G>A (p.Arg130Gln)not specified [RCV004675453]uncertain significance58148929381489293Humanname
597681248CV3611732single nucleotide variantNM_001256732.3(SSBP2):c.523A>G (p.Met175Val)not specified [RCV004857513]uncertain significance58147374781473747Humanname
598174086CV3922855single nucleotide variantNM_001256732.3(SSBP2):c.808A>G (p.Thr270Ala)not specified [RCV005285296]uncertain significance58144271881442718Humanname
598174094CV3922856single nucleotide variantNM_001256732.3(SSBP2):c.837A>C (p.Leu279Phe)not specified [RCV005285297]uncertain significance58144268981442689Humanname
41405582CV981505single nucleotide variantNM_001256732.3(SSBP2):c.971G>C (p.Ser324Thr)not provided [RCV001813073]uncertain significance58143744081437440Humanname