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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


7 records found for search term Tmem72
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8651965CV128540single nucleotide variantNR_033842.1(TMEM72-AS1):n.99-17580G>TLung cancer [RCV000109027]uncertain significance104494080644940806Humanname
8633633CV88848single nucleotide variantNM_001123376.2(TMEM72):c.225C>T (p.Ser75=)Malignant melanoma [RCV000068943]not provided104493365244933652Humanname
8633632CV88847single nucleotide variantNM_001123376.2(TMEM72):c.224C>T (p.Ser75Phe)Malignant melanoma [RCV000068942]not provided104493365144933651Humanname
10395484CV166565single nucleotide variantNM_001123376.3(TMEM72):c.413C>A (p.Ala138Asp)not provided [RCV000190283]not provided104493471944934719Humanname
156381324CV2215453single nucleotide variantNM_001123376.3(TMEM72):c.689G>A (p.Arg230His)not specified [RCV004089252]uncertain significance104493499544934995Humanname
156239517CV2235931single nucleotide variantNM_001123376.3(TMEM72):c.433T>C (p.Ser145Pro)not specified [RCV004113815]likely benign104493473944934739Humanname
155929900CV2360993single nucleotide variantNM_001123376.3(TMEM72):c.469G>A (p.Val157Met)not specified [RCV004216191]uncertain significance104493477544934775Humanname