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


2 records found for search term Als2cr11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8625262CV80381single nucleotide variantNM_001168221.1(ALS2CR11):c.5453G>A (p.Arg1818Lys)Malignant melanoma [RCV000060458]not provided2201487622201487622Humanname
8630130CV85277single nucleotide variantNM_001168221.1(ALS2CR11):c.3596G>A (p.Gly1199Glu)Malignant melanoma [RCV000065359]not provided2201492745201492745Humanname