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Variants search result for Homo sapiens
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23 records found for search term Pggt1b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8580262CV114692single nucleotide variantNM_005023.3(PGGT1B):c.327+1530A>GLung cancer [RCV000095215]uncertain significance5115240009115240009Humanname
598247264CV3999856single nucleotide variantNM_005023.4(PGGT1B):c.7G>T (p.Ala3Ser)not specified [RCV005384154]uncertain significance5115262845115262845Humanname
329362371CV2444650single nucleotide variantNM_005023.4(PGGT1B):c.10A>G (p.Thr4Ala)not specified [RCV004258915]uncertain significance5115262842115262842Humanname
598247314CV3999862single nucleotide variantNM_005023.4(PGGT1B):c.20A>G (p.Glu7Gly)not specified [RCV005384160]uncertain significance5115262832115262832Humanname
156060165CV2280110single nucleotide variantNM_005023.4(PGGT1B):c.35G>T (p.Ser12Ile)not specified [RCV004146763]uncertain significance5115262817115262817Humanname
401888219CV2788150single nucleotide variantNM_005023.4(PGGT1B):c.50G>C (p.Arg17Pro)not specified [RCV004352769]uncertain significance5115262802115262802Humanname
597675569CV3572085single nucleotide variantNM_005023.4(PGGT1B):c.44G>A (p.Gly15Glu)not specified [RCV004836808]uncertain significance5115262808115262808Humanname
598247286CV3999859single nucleotide variantNM_005023.4(PGGT1B):c.46G>A (p.Glu16Lys)not specified [RCV005384157]uncertain significance5115262806115262806Humanname
329399190CV2436346single nucleotide variantNM_005023.4(PGGT1B):c.160G>A (p.Ala54Thr)not specified [RCV004251744]uncertain significance5115253236115253236Humanname
405747848CV3368760single nucleotide variantNM_005023.4(PGGT1B):c.188C>G (p.Ser63Cys)not specified [RCV004498658]uncertain significance5115253208115253208Humanname
597675598CV3572088single nucleotide variantNM_005023.4(PGGT1B):c.148A>G (p.Ile50Val)not specified [RCV004836811]uncertain significance5115253248115253248Humanname
597675612CV3572089single nucleotide variantNM_005023.4(PGGT1B):c.266A>G (p.Asn89Ser)not specified [RCV004836812]uncertain significance5115241600115241600Humanname
598247296CV3999860single nucleotide variantNM_005023.4(PGGT1B):c.208G>A (p.Asp70Asn)not specified [RCV005384158]uncertain significance5115253188115253188Humanname
156106223CV2370868single nucleotide variantNM_005023.4(PGGT1B):c.317A>G (p.Asn106Ser)not specified [RCV004218611]uncertain significance5115241549115241549Humanname
401775085CV2696213single nucleotide variantNM_005023.4(PGGT1B):c.762G>A (p.Met254Ile)not specified [RCV004310255]uncertain significance5115221905115221905Humanname
405747854CV3368761single nucleotide variantNM_005023.4(PGGT1B):c.469G>C (p.Glu157Gln)not specified [RCV004498659]uncertain significance5115237868115237868Humanname
405747862CV3368762single nucleotide variantNM_005023.4(PGGT1B):c.782A>G (p.His261Arg)not specified [RCV004498660]uncertain significance5115221885115221885Humanname
597675580CV3572086single nucleotide variantNM_005023.4(PGGT1B):c.830G>A (p.Gly277Glu)not specified [RCV004836809]uncertain significance5115221837115221837Humanname
598247272CV3999857single nucleotide variantNM_005023.4(PGGT1B):c.577A>G (p.Met193Val)not specified [RCV005384155]uncertain significance5115236425115236425Humanname
598247280CV3999858single nucleotide variantNM_005023.4(PGGT1B):c.667A>G (p.Thr223Ala)not specified [RCV005384156]uncertain significance5115222000115222000Humanname
598196941CV3999863single nucleotide variantNM_005023.4(PGGT1B):c.913C>G (p.Leu305Val)not specified [RCV005397798]uncertain significance5115216904115216904Humanname
156011281CV2362227single nucleotide variantNM_005023.4(PGGT1B):c.1103A>G (p.Gln368Arg)not specified [RCV004210023]uncertain significance5115212433115212433Humanname
401897671CV2776610single nucleotide variantNM_005023.4(PGGT1B):c.1057C>T (p.Arg353Cys)not specified [RCV004357486]uncertain significance5115212479115212479Humanname