Lhx5 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 Lhx5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
13529440	CV503910	single nucleotide variant	NM_022363.3(LHX5):c.675+4C>A	not specified [RCV000600310]	likely benign	12	113468123	113468123	Human		name
407492370	CV3448919	single nucleotide variant	NM_022363.3(LHX5):c.29G>T (p.Arg10Leu)	not specified [RCV004642471]	uncertain significance	12	113471470	113471470	Human		name
155926384	CV2345173	single nucleotide variant	NM_022363.3(LHX5):c.143G>A (p.Gly48Asp)	not specified [RCV004195913]	uncertain significance	12	113471356	113471356	Human		name
405654640	CV3276690	single nucleotide variant	NM_022363.3(LHX5):c.113A>G (p.Asn38Ser)	not specified [RCV004415035]	uncertain significance	12	113471386	113471386	Human		name
405654645	CV3276692	single nucleotide variant	NM_022363.3(LHX5):c.233G>T (p.Arg78Leu)	not specified [RCV004415037]	uncertain significance	12	113469286	113469286	Human		name
156321296	CV2197551	single nucleotide variant	NM_022363.3(LHX5):c.871A>G (p.Ser291Gly)	not specified [RCV004081272]	likely benign	12	113463528	113463528	Human		name
155991167	CV2256412	single nucleotide variant	NM_022363.3(LHX5):c.754T>C (p.Phe252Leu)	not specified [RCV004116849]	uncertain significance	12	113467343	113467343	Human		name
156200541	CV2350861	single nucleotide variant	NM_022363.3(LHX5):c.310G>C (p.Glu104Gln)	not specified [RCV004211699]	uncertain significance	12	113469209	113469209	Human		name
156141280	CV2383679	single nucleotide variant	NM_022363.3(LHX5):c.625A>G (p.Ile209Val)	not specified [RCV004231569]	uncertain significance	12	113468177	113468177	Human		name
401747932	CV2687638	single nucleotide variant	NM_022363.3(LHX5):c.821C>G (p.Thr274Ser)	not specified [RCV004300853]	uncertain significance	12	113467276	113467276	Human		name
401783742	CV2723902	single nucleotide variant	NM_022363.3(LHX5):c.772A>C (p.Met258Leu)	not specified [RCV004326032]	uncertain significance	12	113467325	113467325	Human		name
401875232	CV2787611	single nucleotide variant	NM_022363.3(LHX5):c.914A>C (p.Gln305Pro)	not specified [RCV004356548]	uncertain significance	12	113463485	113463485	Human		name
405654648	CV3276693	single nucleotide variant	NM_022363.3(LHX5):c.748G>C (p.Ala250Pro)	not specified [RCV004415038]	uncertain significance	12	113467349	113467349	Human		name
405654653	CV3276695	single nucleotide variant	NM_022363.3(LHX5):c.895G>C (p.Gly299Arg)	not specified [RCV004415040]	uncertain significance	12	113463504	113463504	Human		name
407460848	CV3448917	single nucleotide variant	NM_022363.3(LHX5):c.772A>T (p.Met258Leu)	not specified [RCV004633973]	uncertain significance	12	113467325	113467325	Human		name
407492367	CV3448918	single nucleotide variant	NM_022363.3(LHX5):c.974C>A (p.Ala325Glu)	not specified [RCV004642470]	uncertain significance	12	113463425	113463425	Human		name
597641963	CV3696291	single nucleotide variant	NM_022363.3(LHX5):c.892C>A (p.His298Asn)	not specified [RCV004941808]	uncertain significance	12	113463507	113463507	Human		name
598230074	CV3984603	single nucleotide variant	NM_022363.3(LHX5):c.351C>A (p.Asp117Glu)	not specified [RCV005362648]	uncertain significance	12	113469168	113469168	Human		name
598237026	CV3984605	single nucleotide variant	NM_022363.3(LHX5):c.533C>T (p.Thr178Ile)	not specified [RCV005363995]	uncertain significance	12	113468269	113468269	Human		name
156363913	CV2262730	single nucleotide variant	NM_022363.3(LHX5):c.1087C>A (p.Pro363Thr)	not specified [RCV004130915]	uncertain significance	12	113463312	113463312	Human		name
156290333	CV2309811	single nucleotide variant	NM_022363.3(LHX5):c.1067G>A (p.Gly356Asp)	not specified [RCV004160929]	uncertain significance	12	113463332	113463332	Human		name
401752513	CV2682845	single nucleotide variant	NM_022363.3(LHX5):c.1090A>G (p.Met364Val)	not specified [RCV004283647]	uncertain significance	12	113463309	113463309	Human		name
405654634	CV3276688	single nucleotide variant	NM_022363.3(LHX5):c.1073C>A (p.Pro358Gln)	not specified [RCV004415033]	uncertain significance	12	113463326	113463326	Human		name
405654637	CV3276689	single nucleotide variant	NM_022363.3(LHX5):c.1099G>A (p.Glu367Lys)	not specified [RCV004415034]	uncertain significance	12	113463300	113463300	Human		name
405654643	CV3276691	single nucleotide variant	NM_022363.3(LHX5):c.1150G>A (p.Gly384Ser)	not specified [RCV004415036]	uncertain significance	12	113463249	113463249	Human		name
407460853	CV3448921	single nucleotide variant	NM_022363.3(LHX5):c.1186C>A (p.Leu396Ile)	not specified [RCV004633974]	uncertain significance	12	113463213	113463213	Human		name
598237016	CV3984601	single nucleotide variant	NM_022363.3(LHX5):c.1004C>T (p.Ala335Val)	not specified [RCV005363993]	uncertain significance	12	113463395	113463395	Human		name
598237020	CV3984602	single nucleotide variant	NM_022363.3(LHX5):c.1135A>C (p.Met379Leu)	not specified [RCV005363994]	uncertain significance	12	113463264	113463264	Human		name
598260460	CV3984604	single nucleotide variant	NM_022363.3(LHX5):c.1060G>A (p.Glu354Lys)	not specified [RCV005347626]	uncertain significance	12	113463339	113463339	Human		name

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