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Variants search result for Homo sapiens
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26 records found for search term Pdcd1lg2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597698296CV3568650single nucleotide variantNM_025239.4(PDCD1LG2):c.5T>A (p.Ile2Asn)not specified [RCV004839445]uncertain significance955225515522551Humanname
329371891CV2454973single nucleotide variantNM_025239.4(PDCD1LG2):c.52G>C (p.Ala18Pro)not specified [RCV004272242]uncertain significance955225985522598Humanname
405775112CV3375088single nucleotide variantNM_025239.4(PDCD1LG2):c.53C>T (p.Ala18Val)not specified [RCV004502964]uncertain significance955225995522599Humanname
155978775CV2266552single nucleotide variantNM_025239.4(PDCD1LG2):c.164T>C (p.Ile55Thr)not specified [RCV004131107]uncertain significance955348535534853Humanname
156165770CV2315191single nucleotide variantNM_025239.4(PDCD1LG2):c.163A>C (p.Ile55Leu)not specified [RCV004165363]likely benign955348525534852Humanname
405775089CV3375084single nucleotide variantNM_025239.4(PDCD1LG2):c.211G>A (p.Glu71Lys)not specified [RCV004502960]uncertain significance955349005534900Humanname
405775095CV3375085single nucleotide variantNM_025239.4(PDCD1LG2):c.271C>G (p.Gln91Glu)not specified [RCV004502961]uncertain significance955349605534960Humanname
598165637CV4006136single nucleotide variantNM_025239.4(PDCD1LG2):c.263A>G (p.His88Arg)not specified [RCV005391363]uncertain significance955349525534952Humanname
598165648CV4006138single nucleotide variantNM_025239.4(PDCD1LG2):c.169G>C (p.Ala57Pro)not specified [RCV005391365]uncertain significance955348585534858Humanname
156317243CV2203939single nucleotide variantNM_025239.4(PDCD1LG2):c.448C>G (p.Leu150Val)not specified [RCV004069987]uncertain significance955494215549421Humanname
156114611CV2208929single nucleotide variantNM_025239.4(PDCD1LG2):c.595G>A (p.Val199Met)not specified [RCV004085288]likely benign955495685549568Humanname
156123899CV2227296single nucleotide variantNM_025239.4(PDCD1LG2):c.776A>C (p.Lys259Thr)not specified [RCV004091853]uncertain significance955631715563171Humanname
156193563CV2296988single nucleotide variantNM_025239.4(PDCD1LG2):c.378A>G (p.Ile126Met)not specified [RCV004150917]uncertain significance955493515549351Humanname
156061680CV2380273single nucleotide variantNM_025239.4(PDCD1LG2):c.442T>A (p.Tyr148Asn)not specified [RCV004224628]uncertain significance955494155549415Humanname
155907873CV2387144single nucleotide variantNM_025239.4(PDCD1LG2):c.740T>A (p.Leu247His)not specified [RCV004238253]uncertain significance955577265557726Humanname
401860562CV2758525single nucleotide variantNM_025239.4(PDCD1LG2):c.817A>G (p.Ile273Val)not specified [RCV004337617]uncertain significance955699545569954Humanname
401893710CV2765419single nucleotide variantNM_025239.4(PDCD1LG2):c.643C>T (p.Pro215Ser)not specified [RCV004341740]uncertain significance955576295557629Humanname
405775101CV3375086single nucleotide variantNM_025239.4(PDCD1LG2):c.390C>G (p.Ile130Met)not specified [RCV004502962]uncertain significance955493635549363Humanname
405775107CV3375087single nucleotide variantNM_025239.4(PDCD1LG2):c.440G>A (p.Gly147Asp)not specified [RCV004502963]uncertain significance955494135549413Humanname
405775118CV3375089single nucleotide variantNM_025239.4(PDCD1LG2):c.554C>T (p.Pro185Leu)not specified [RCV004502965]uncertain significance955495275549527Humanname
597698286CV3568649single nucleotide variantNM_025239.4(PDCD1LG2):c.775A>G (p.Lys259Glu)not specified [RCV004839444]uncertain significance955631705563170Humanname
597698305CV3568651single nucleotide variantNM_025239.4(PDCD1LG2):c.389T>C (p.Ile130Thr)not specified [RCV004839446]uncertain significance955493625549362Humanname
597698313CV3568652single nucleotide variantNM_025239.4(PDCD1LG2):c.299A>C (p.Tyr100Ser)not specified [RCV004839447]uncertain significance955349885534988Humanname
598165629CV4006134single nucleotide variantNM_025239.4(PDCD1LG2):c.431A>T (p.Gln144Leu)not specified [RCV005391362]uncertain significance955494045549404Humanname
598196076CV4006135single nucleotide variantNM_025239.4(PDCD1LG2):c.613G>A (p.Ala205Thr)not specified [RCV005397644]uncertain significance955495865549586Humanname
598165654CV4006139single nucleotide variantNM_025239.4(PDCD1LG2):c.396G>C (p.Lys132Asn)not specified [RCV005391366]uncertain significance955493695549369Humanname