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Variants search result for Homo sapiens
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15 records found for search term Ppp6c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156276217CV2316519single nucleotide variantNM_002721.5(PPP6C):c.75+67C>Tnot specified [RCV004169987]uncertain significance9125189577125189577Humanname
401767299CV2681593single nucleotide variantNM_002721.5(PPP6C):c.75+65C>Tnot specified [RCV004292114]uncertain significance9125189579125189579Humanname
407529923CV3467862single nucleotide variantNM_002721.5(PPP6C):c.75+47C>Gnot specified [RCV004656326]uncertain significance9125189597125189597Humanname
597769982CV3584154single nucleotide variantNM_002721.5(PPP6C):c.75+80C>Tnot specified [RCV004851032]likely benign9125189564125189564Humanname
156133503CV2216807single nucleotide variantNM_002721.5(PPP6C):c.21C>G (p.Asp7Glu)not specified [RCV004083244]uncertain significance9125189698125189698Humanname
155947900CV2271904single nucleotide variantNM_002721.5(PPP6C):c.26A>G (p.Tyr9Cys)not specified [RCV004124731]uncertain significance9125189693125189693Humanname
405653248CV3377152single nucleotide variantNM_002721.5(PPP6C):c.15C>A (p.Asp5Glu)not specified [RCV004510187]uncertain significance9125189704125189704Humanname
598176256CV3891175single nucleotide variantNM_002721.5(PPP6C):c.171G>A (p.Gln57=)not provided [RCV005252025]not provided9125171085125171085Humanname
15108875CV723329single nucleotide variantNM_002721.5(PPP6C):c.609T>C (p.Asp203=)not provided [RCV000893754]benign9125153593125153593Humanname
156069373CV2203780single nucleotide variantNM_002721.5(PPP6C):c.181C>G (p.Leu61Val)not specified [RCV004074422]uncertain significance9125160897125160897Humanname
407529924CV3467863single nucleotide variantNM_002721.5(PPP6C):c.274A>G (p.Thr92Ala)not specified [RCV004656327]uncertain significance9125158346125158346Humanname
597769972CV3584152single nucleotide variantNM_002721.5(PPP6C):c.896C>T (p.Thr299Met)not specified [RCV004851030]uncertain significance9125149695125149695Humanname
597769977CV3584153single nucleotide variantNM_002721.5(PPP6C):c.693A>T (p.Lys231Asn)not specified [RCV004851031]uncertain significance9125149898125149898Humanname
597769986CV3584155single nucleotide variantNM_002721.5(PPP6C):c.502C>G (p.Pro168Ala)not specified [RCV004851033]uncertain significance9125153700125153700Humanname
12840312CV363387single nucleotide variantNM_002721.5(PPP6C):c.790C>T (p.Arg264Cys)Malignant melanoma of skin [RCV000430465]|Squamous cell lung carcinoma [RCV000437241]likely pathogenic9125149801125149801Human2name