Nme2 Variant Search Result - Rat Genome Database

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6 records found for search term Nme2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597653932	CV3566255	single nucleotide variant	NM_002512.4(NME2):c.36G>C (p.Lys12Asn)	not specified [RCV004827197]	uncertain significance	17	51166866	51166866	Human		name
405270753	CV3219780	single nucleotide variant	NM_001018136.3(NME1-NME2):c.21C>A (p.Thr7=)	NME1-NME2-related disorder [RCV003971517]	likely benign	17	51155675	51155675	Human		name , trait , alternate_id
401935814	CV2811523	single nucleotide variant	NM_001018136.3(NME1-NME2):c.705T>C (p.Ser235=)	not provided [RCV003413276]	likely benign	17	51171505	51171505	Human		name
598206076	CV4004336	single nucleotide variant	NM_001018136.3(NME1-NME2):c.101G>A (p.Arg34His)	not specified [RCV005376856]	uncertain significance	17	51155755	51155755	Human		name
407481903	CV3458871	single nucleotide variant	NM_001018136.3(NME1-NME2):c.557G>T (p.Gly186Val)	not specified [RCV004647403]	uncertain significance	17	51168327	51168327	Human		name
15153383	CV745310	single nucleotide variant	NM_000269.3(NME1):c.341+10T>G	NME1-NME2-related disorder [RCV003932834]\|not provided [RCV000901750]	benign	17	51161282	51161282	Human		trait , alternate_id