Lbx2 Variant Search Result - Rat Genome Database

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17 records found for search term Lbx2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15168390	CV697671	single nucleotide variant	NM_001282430.2(LBX2):c.51A>T (p.Ala17=)	not provided [RCV000949246]	benign	2	74499487	74499487	Human		name
156090206	CV2344633	single nucleotide variant	NM_001009812.2(LBX2):c.43G>C (p.Gly15Arg)	not specified [RCV004197402]	uncertain significance	2	74502817	74502817	Human		name
15187391	CV763443	single nucleotide variant	NM_001282430.2(LBX2):c.387G>C (p.Val129=)	not provided [RCV000931643]	likely benign	2	74498137	74498137	Human		name
155984123	CV2344383	single nucleotide variant	NM_001282430.2(LBX2):c.214G>C (p.Gly72Arg)	not specified [RCV004195135]	uncertain significance	2	74498310	74498310	Human		name
405815333	CV3283730	single nucleotide variant	NM_001282430.2(LBX2):c.238C>T (p.Pro80Ser)	not specified [RCV004410318]	uncertain significance	2	74498286	74498286	Human		name
405815334	CV3283731	single nucleotide variant	NM_001282430.2(LBX2):c.260A>G (p.Lys87Arg)	not specified [RCV004410319]	uncertain significance	2	74498264	74498264	Human		name
597631855	CV3698668	single nucleotide variant	NM_001282430.2(LBX2):c.218C>G (p.Pro73Arg)	not specified [RCV004939875]	uncertain significance	2	74498306	74498306	Human		name
598198025	CV3987776	single nucleotide variant	NM_001282430.2(LBX2):c.230G>C (p.Gly77Ala)	not specified [RCV005355435]	uncertain significance	2	74498294	74498294	Human		name
155912011	CV2235481	single nucleotide variant	NM_001282430.2(LBX2):c.535G>A (p.Gly179Ser)	not specified [RCV004109524]	uncertain significance	2	74497989	74497989	Human		name
155966998	CV2329864	single nucleotide variant	NM_001282430.2(LBX2):c.584A>C (p.Gln195Pro)	not specified [RCV004183322]	uncertain significance	2	74497940	74497940	Human		name
156181974	CV2338164	single nucleotide variant	NM_001282430.2(LBX2):c.476C>T (p.Pro159Leu)	not specified [RCV004184192]	uncertain significance	2	74498048	74498048	Human		name
329371737	CV2442880	single nucleotide variant	NM_001282430.2(LBX2):c.542C>T (p.Ala181Val)	not specified [RCV004253487]	uncertain significance	2	74497982	74497982	Human		name
401779565	CV2731889	single nucleotide variant	NM_001282430.2(LBX2):c.364C>T (p.Leu122Phe)	not specified [RCV004333134]	uncertain significance	2	74498160	74498160	Human		name
407491166	CV3452460	single nucleotide variant	NM_001282430.2(LBX2):c.478G>A (p.Glu160Lys)	not specified [RCV004642149]	uncertain significance	2	74498046	74498046	Human		name
597631858	CV3698669	single nucleotide variant	NM_001282430.2(LBX2):c.386T>C (p.Val129Ala)	not specified [RCV004939876]	uncertain significance	2	74498138	74498138	Human		name
598174924	CV3987777	single nucleotide variant	NM_001282430.2(LBX2):c.532C>G (p.Leu178Val)	not specified [RCV005371193]	uncertain significance	2	74497992	74497992	Human		name
598198034	CV3987778	single nucleotide variant	NM_001282430.2(LBX2):c.589G>C (p.Asp197His)	not specified [RCV005355436]	uncertain significance	2	74497935	74497935	Human		name