Nub1 Variant Search Result - Rat Genome Database

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18 records found for search term Nub1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401923929	CV2823360	single nucleotide variant	NM_001243351.2(NUB1):c.598+6C>T	not provided [RCV003435311]	likely benign	7	151355956	151355956	Human		name
401909144	CV2823359	single nucleotide variant	NM_001243351.2(NUB1):c.240G>A (p.Thr80=)	not provided [RCV003423838]	likely benign	7	151349195	151349195	Human		name
15189735	CV699947	single nucleotide variant	NM_001243351.2(NUB1):c.12G>T (p.Lys4Asn)	not provided [RCV000954268]	benign	7	151345361	151345361	Human	1	name
15189735	CV699947	single nucleotide variant	NM_001243351.2(NUB1):c.12G>T (p.Lys4Asn)	not provided [RCV000954268]	benign	7	151345361	151345362	Human	1	name
405728546	CV3355790	single nucleotide variant	NM_001243351.2(NUB1):c.200C>A (p.Ala67Glu)	not specified [RCV004496086]	uncertain significance	7	151349155	151349155	Human		name
401894987	CV2792654	single nucleotide variant	NM_001243351.2(NUB1):c.712G>A (p.Gly238Arg)	not specified [RCV004365443]	uncertain significance	7	151360159	151360159	Human		name
405728554	CV3355791	single nucleotide variant	NM_001243351.2(NUB1):c.422C>T (p.Thr141Ile)	not specified [RCV004496087]	uncertain significance	7	151355774	151355774	Human		name
407477447	CV3462242	single nucleotide variant	NM_001243351.2(NUB1):c.509A>G (p.Gln170Arg)	not specified [RCV004638814]	uncertain significance	7	151355861	151355861	Human		name
597643538	CV3573467	single nucleotide variant	NM_001243351.2(NUB1):c.542T>C (p.Leu181Pro)	not specified [RCV004832624]	uncertain significance	7	151355894	151355894	Human		name
156051689	CV2269376	single nucleotide variant	NM_001243351.2(NUB1):c.1555G>T (p.Val519Phe)	not specified [RCV004124507]	uncertain significance	7	151376697	151376697	Human		name
156184871	CV2335752	single nucleotide variant	NM_001243351.2(NUB1):c.1654C>T (p.Pro552Ser)	not specified [RCV004193948]	uncertain significance	7	151376796	151376796	Human		name
156097990	CV2384995	single nucleotide variant	NM_001243351.2(NUB1):c.1568C>T (p.Ala523Val)	not specified [RCV004228267]	uncertain significance	7	151376710	151376710	Human		name
405728531	CV3355789	single nucleotide variant	NM_001243351.2(NUB1):c.1495G>A (p.Val499Met)	not specified [RCV004496085]	uncertain significance	7	151376637	151376637	Human		name
597709252	CV3573465	single nucleotide variant	NM_001243351.2(NUB1):c.1249G>C (p.Glu417Gln)	not specified [RCV004840652]	uncertain significance	7	151374097	151374097	Human		name
597709261	CV3573466	single nucleotide variant	NM_001243351.2(NUB1):c.1466G>A (p.Ser489Asn)	not specified [RCV004840653]	uncertain significance	7	151375918	151375918	Human		name
597709269	CV3573468	single nucleotide variant	NM_001243351.2(NUB1):c.1049A>C (p.Asn350Thr)	not specified [RCV004840654]	uncertain significance	7	151367922	151367922	Human		name
598265495	CV3995027	single nucleotide variant	NM_001243351.2(NUB1):c.1009G>A (p.Val337Ile)	not specified [RCV005387956]	uncertain significance	7	151367882	151367882	Human		name
598233540	CV3995028	single nucleotide variant	NM_001243351.2(NUB1):c.1580C>G (p.Ala527Gly)	not specified [RCV005381737]	uncertain significance	7	151376722	151376722	Human		name