Ncr1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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29 records found for search term Ncr1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156007740	CV2299767	single nucleotide variant	NM_004829.7(NCR1):c.10A>G (p.Thr4Ala)	not specified [RCV004148925]	uncertain significance	19	54906197	54906197	Human		name
405813955	CV3344984	single nucleotide variant	NM_004829.7(NCR1):c.88T>G (p.Phe30Val)	not specified [RCV004484117]	uncertain significance	19	54906540	54906540	Human		name
38467679	CV920964	single nucleotide variant	NM_004829.7(NCR1):c.339G>A (p.Leu113=)	not provided [RCV001200422]	likely benign	19	54906791	54906791	Human		name
155983741	CV2240771	single nucleotide variant	NM_004829.7(NCR1):c.182A>G (p.His61Arg)	not specified [RCV004119380]	uncertain significance	19	54906634	54906634	Human		name
156184135	CV2292210	single nucleotide variant	NM_004829.7(NCR1):c.263T>G (p.Met88Arg)	not specified [RCV004148254]	uncertain significance	19	54906715	54906715	Human		name
156156644	CV2368075	single nucleotide variant	NM_004829.7(NCR1):c.271C>T (p.Arg91Cys)	not specified [RCV004216428]	uncertain significance	19	54906723	54906723	Human		name
329390899	CV2455577	single nucleotide variant	NM_004829.7(NCR1):c.127A>G (p.Lys43Glu)	not specified [RCV004276828]	uncertain significance	19	54906579	54906579	Human		name
405813892	CV3344952	single nucleotide variant	NM_004829.7(NCR1):c.181C>G (p.His61Asp)	not specified [RCV004484085]	uncertain significance	19	54906633	54906633	Human		name
405813902	CV3344957	single nucleotide variant	NM_004829.7(NCR1):c.226G>C (p.Glu76Gln)	not specified [RCV004484090]	uncertain significance	19	54906678	54906678	Human		name
407488820	CV3454587	single nucleotide variant	NM_004829.7(NCR1):c.181C>A (p.His61Asn)	not specified [RCV004641367]	uncertain significance	19	54906633	54906633	Human		name
597667957	CV3558853	single nucleotide variant	NM_004829.7(NCR1):c.226G>A (p.Glu76Lys)	not specified [RCV004829394]	uncertain significance	19	54906678	54906678	Human		name
598217811	CV4003924	single nucleotide variant	NM_004829.7(NCR1):c.193A>G (p.Ser65Gly)	not specified [RCV005379177]	uncertain significance	19	54906645	54906645	Human		name
598253592	CV4003925	single nucleotide variant	NM_004829.7(NCR1):c.257C>T (p.Pro86Leu)	not specified [RCV005385365]	uncertain significance	19	54906709	54906709	Human		name
156004792	CV2296028	single nucleotide variant	NM_004829.7(NCR1):c.482C>T (p.Ser161Phe)	not specified [RCV004151908]	uncertain significance	19	54909371	54909371	Human		name
156260977	CV2322337	single nucleotide variant	NM_004829.7(NCR1):c.773G>A (p.Arg258Gln)	not specified [RCV004176092]	uncertain significance	19	54912729	54912729	Human		name
156063848	CV2349678	single nucleotide variant	NM_004829.7(NCR1):c.644A>G (p.Glu215Gly)	not specified [RCV004204094]	likely benign	19	54910027	54910027	Human		name
329362191	CV2448394	single nucleotide variant	NM_004829.7(NCR1):c.566G>A (p.Arg189Gln)	not specified [RCV004256679]	uncertain significance	19	54909455	54909455	Human		name
329396892	CV2463605	single nucleotide variant	NM_004829.7(NCR1):c.331A>G (p.Asn111Asp)	not specified [RCV004277404]	likely benign	19	54906783	54906783	Human		name
405813919	CV3344965	single nucleotide variant	NM_004829.7(NCR1):c.442A>C (p.Thr148Pro)	not specified [RCV004484098]	uncertain significance	19	54909331	54909331	Human		name
405813932	CV3344972	single nucleotide variant	NM_004829.7(NCR1):c.494A>G (p.Gln165Arg)	not specified [RCV004484105]	uncertain significance	19	54909383	54909383	Human		name
405813951	CV3344982	single nucleotide variant	NM_004829.7(NCR1):c.802G>T (p.Ala268Ser)	not specified [RCV004484115]	uncertain significance	19	54912758	54912758	Human		name
407525736	CV3454586	single nucleotide variant	NM_004829.7(NCR1):c.764A>G (p.Asn255Ser)	not specified [RCV004654583]	uncertain significance	19	54912720	54912720	Human		name
407525739	CV3454588	single nucleotide variant	NM_004829.7(NCR1):c.426C>G (p.Phe142Leu)	not specified [RCV004654584]	uncertain significance	19	54909315	54909315	Human		name
407489122	CV3454589	single nucleotide variant	NM_004829.7(NCR1):c.533G>A (p.Gly178Asp)	not specified [RCV004641368]	uncertain significance	19	54909422	54909422	Human		name
597667949	CV3558852	single nucleotide variant	NM_004829.7(NCR1):c.554G>A (p.Arg185Lys)	not specified [RCV004829393]	uncertain significance	19	54909443	54909443	Human		name
597667967	CV3558854	single nucleotide variant	NM_004829.7(NCR1):c.521A>C (p.Glu174Ala)	not specified [RCV004829395]	uncertain significance	19	54909410	54909410	Human		name
597667975	CV3558855	single nucleotide variant	NM_004829.7(NCR1):c.853G>A (p.Glu285Lys)	not specified [RCV004829396]	uncertain significance	19	54912809	54912809	Human		name
597667983	CV3558856	single nucleotide variant	NM_004829.7(NCR1):c.695G>A (p.Gly232Asp)	not specified [RCV004829397]	likely benign	19	54912180	54912180	Human		name
598217805	CV4003923	single nucleotide variant	NM_004829.7(NCR1):c.407C>T (p.Ser136Leu)	not specified [RCV005379176]	uncertain significance	19	54909296	54909296	Human		name

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