Ncald Variant Search Result - Rat Genome Database

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9 records found for search term Ncald

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401904914	CV2821200	deletion	NM_001040630.2(NCALD):c.-123+73del	not provided [RCV003435574]	benign	8	102124497	102124497	Human		name
401904915	CV2821201	single nucleotide variant	NM_001040630.2(NCALD):c.-123+64A>T	not provided [RCV003435575]	likely benign	8	102124506	102124506	Human		name
8649687	CV126261	single nucleotide variant	NM_001040624.1(NCALD):c.-157+6930C>T	Lung cancer [RCV000106748]	uncertain significance	8	102013307	102013307	Human		name
597647509	CV3562209	single nucleotide variant	NM_032041.3(NCALD):c.199C>T (p.His67Tyr)	not specified [RCV004826423]	uncertain significance	8	101719431	101719431	Human		name
156068412	CV2381170	single nucleotide variant	NM_032041.3(NCALD):c.439A>G (p.Lys147Glu)	not specified [RCV004227244]	uncertain significance	8	101692836	101692836	Human		name
405787174	CV3339845	single nucleotide variant	NM_032041.3(NCALD):c.415C>G (p.Pro139Ala)	not specified [RCV004473081]	uncertain significance	8	101692860	101692860	Human		name
405787210	CV3339853	single nucleotide variant	NM_032041.3(NCALD):c.456C>G (p.Ile152Met)	not specified [RCV004473089]	uncertain significance	8	101692819	101692819	Human		name
405787231	CV3339857	single nucleotide variant	NM_032041.3(NCALD):c.535A>G (p.Ile179Val)	not specified [RCV004473093]	uncertain significance	8	101689356	101689356	Human		name
8632751	CV87966	single nucleotide variant	NM_001040624.1(NCALD):c.559C>T (p.Pro187Ser)	Malignant melanoma [RCV000068058]	not provided	8	101689332	101689332	Human		name