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Variants search result for Homo sapiens
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28 records found for search term Ppm1l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8578262CV112641single nucleotide variantNM_139245.2(PPM1L):c.399+92441G>CLung cancer [RCV000093164]uncertain significance3160849148160849148Humanname
8578263CV112642single nucleotide variantNM_139245.2(PPM1L):c.400-35046C>ALung cancer [RCV000093165]uncertain significance3160926690160926690Humanname
8578264CV112643single nucleotide variantNM_139245.2(PPM1L):c.575-19681A>GLung cancer [RCV000093166]uncertain significance3161045722161045722Humanname
156186120CV2377920single nucleotide variantNM_139245.4(PPM1L):c.76C>G (p.Leu26Val)not specified [RCV004230488]uncertain significance3160756384160756384Humanname
155995915CV2283550single nucleotide variantNM_139245.4(PPM1L):c.258G>C (p.Trp86Cys)not specified [RCV004140066]uncertain significance3160756566160756566Humanname
329374337CV2434781single nucleotide variantNM_139245.4(PPM1L):c.158G>A (p.Arg53Gln)not specified [RCV004248477]uncertain significance3160756466160756466Humanname
405794940CV3366506single nucleotide variantNM_139245.4(PPM1L):c.218G>C (p.Gly73Ala)not specified [RCV004507208]uncertain significance3160756526160756526Humanname
405794943CV3366507single nucleotide variantNM_139245.4(PPM1L):c.270C>G (p.Asn90Lys)not specified [RCV004507209]uncertain significance3160756578160756578Humanname
597758359CV3591371single nucleotide variantNM_139245.4(PPM1L):c.166G>A (p.Val56Met)not specified [RCV004848517]uncertain significance3160756474160756474Humanname
156289959CV2299427single nucleotide variantNM_139245.4(PPM1L):c.493T>C (p.Tyr165His)not specified [RCV004154511]uncertain significance3160961829160961829Humanname
155912912CV2305181single nucleotide variantNM_139245.4(PPM1L):c.392G>C (p.Gly131Ala)not specified [RCV004171119]uncertain significance3160756700160756700Humanname
156060782CV2305435single nucleotide variantNM_139245.4(PPM1L):c.587T>C (p.Leu196Ser)not specified [RCV004165159]uncertain significance3161065415161065415Humanname
155916226CV2336109single nucleotide variantNM_139245.4(PPM1L):c.778A>G (p.Ile260Val)not specified [RCV004189704]uncertain significance3161068852161068852Humanname
329395216CV2458215single nucleotide variantNM_139245.4(PPM1L):c.421T>C (p.Ser141Pro)not specified [RCV004265877]uncertain significance3160961757160961757Humanname
405794946CV3366508single nucleotide variantNM_139245.4(PPM1L):c.347C>T (p.Ala116Val)not specified [RCV004507210]uncertain significance3160756655160756655Humanname
405794949CV3366509single nucleotide variantNM_139245.4(PPM1L):c.463G>A (p.Glu155Lys)not specified [RCV004507211]uncertain significance3160961799160961799Humanname
405794952CV3366510single nucleotide variantNM_139245.4(PPM1L):c.704A>G (p.Gln235Arg)not specified [RCV004507212]uncertain significance3161065532161065532Humanname
405794955CV3366511single nucleotide variantNM_139245.4(PPM1L):c.811C>T (p.Pro271Ser)not specified [RCV004507213]uncertain significance3161068885161068885Humanname
405794958CV3366512single nucleotide variantNM_139245.4(PPM1L):c.812C>T (p.Pro271Leu)not specified [RCV004507214]uncertain significance3161068886161068886Humanname
407482983CV3471514single nucleotide variantNM_139245.4(PPM1L):c.385G>A (p.Gly129Arg)not specified [RCV004664867]uncertain significance3160756693160756693Humanname
407529715CV3471515single nucleotide variantNM_139245.4(PPM1L):c.938C>T (p.Ala313Val)not specified [RCV004656179]uncertain significance3161069012161069012Humanname
407529717CV3471516single nucleotide variantNM_139245.4(PPM1L):c.796T>A (p.Ser266Thr)not specified [RCV004656180]uncertain significance3161068870161068870Humanname
597758348CV3591369single nucleotide variantNM_139245.4(PPM1L):c.866T>A (p.Leu289Gln)not specified [RCV004848515]uncertain significance3161068940161068940Humanname
597758354CV3591370single nucleotide variantNM_139245.4(PPM1L):c.527T>C (p.Ile176Thr)not specified [RCV004848516]uncertain significance3160961863160961863Humanname
597758369CV3591373single nucleotide variantNM_139245.4(PPM1L):c.425G>A (p.Arg142Gln)not specified [RCV004848519]uncertain significance3160961761160961761Humanname
598168959CV3897494single nucleotide variantNM_139245.4(PPM1L):c.526A>G (p.Ile176Val)not specified [RCV005262706]uncertain significance3160961862160961862Humanname
329362069CV2448268single nucleotide variantNM_139245.4(PPM1L):c.1014A>C (p.Arg338Ser)not specified [RCV004263467]uncertain significance3161069088161069088Humanname
405794935CV3366505single nucleotide variantNM_139245.4(PPM1L):c.1030A>G (p.Ile344Val)not specified [RCV004507207]uncertain significance3161069104161069104Humanname