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


7 records found for search term Pak7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8586657CV121261single nucleotide variantNM_020341.3(PAK7):c.990+4374C>ALung cancer [RCV000101781]uncertain significance2095757719575771Humanname
8586658CV121262single nucleotide variantNM_020341.3(PAK7):c.204+1124A>GLung cancer [RCV000101782]uncertain significance2096430019643001Humanname
8586659CV121263single nucleotide variantNM_020341.3(PAK7):c.-162+34146G>TLung cancer [RCV000101783]uncertain significance2097845349784534Humanname
8637452CV92678single nucleotide variantNM_020341.3(PAK7):c.666C>A (p.Ala222=)Malignant melanoma [RCV000072776]not provided2095804699580469Humanname
8637451CV92677single nucleotide variantNM_020341.3(PAK7):c.1320C>T (p.Val440=)Malignant melanoma [RCV000072775]not provided2095660559566055Humanname
8628584CV83728single nucleotide variantNM_020341.3(PAK7):c.961T>G (p.Leu321Val)Malignant melanoma [RCV000063809]not provided2095801749580174Humanname
8628583CV83727single nucleotide variantNM_020341.3(PAK7):c.1498G>A (p.Asp500Asn)Malignant melanoma [RCV000063808]not provided2095630099563009Humanname