Lxn Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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18 records found for search term Lxn

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
38461463	CV920188	single nucleotide variant	NM_020169.4(LXN):c.570+1G>C	See cases [RCV001197651]	uncertain significance	3	158667011	158667011	Human		name
155912892	CV2305166	single nucleotide variant	NM_020169.4(LXN):c.52C>G (p.Gln18Glu)	not specified [RCV004171106]	likely benign	3	158672427	158672427	Human		name
329360680	CV2439592	single nucleotide variant	NM_020169.4(LXN):c.80C>T (p.Thr27Ile)	not specified [RCV004255611]	uncertain significance	3	158672399	158672399	Human		name
407481075	CV3449316	single nucleotide variant	NM_020169.4(LXN):c.65A>G (p.Asn22Ser)	not specified [RCV004640301]	uncertain significance	3	158672414	158672414	Human		name
15201250	CV697915	single nucleotide variant	NM_020169.4(LXN):c.46G>A (p.Val16Met)	not provided [RCV000957567]	likely benign	3	158672433	158672433	Human	1	name
15201250	CV697915	single nucleotide variant	NM_020169.4(LXN):c.46G>A (p.Val16Met)	not provided [RCV000957567]	likely benign	3	158672433	158672434	Human	1	name
15202449	CV720279	single nucleotide variant	NM_020169.4(LXN):c.501G>A (p.Lys167=)	not provided [RCV000891476]	benign	3	158669002	158669002	Human		name
15184725	CV720281	single nucleotide variant	NM_020169.4(LXN):c.38C>T (p.Ala13Val)	not provided [RCV000886512]	benign	3	158672441	158672441	Human		name
407481069	CV3449314	single nucleotide variant	NM_020169.4(LXN):c.208T>C (p.Cys70Arg)	not specified [RCV004640299]	uncertain significance	3	158669595	158669595	Human		name
597644727	CV3699892	single nucleotide variant	NM_020169.4(LXN):c.187C>A (p.Gln63Lys)	not specified [RCV004942247]	uncertain significance	3	158670962	158670962	Human		name
598182473	CV3981363	single nucleotide variant	NM_020169.4(LXN):c.264C>A (p.Asn88Lys)	not specified [RCV005372750]	uncertain significance	3	158669539	158669539	Human		name
15177552	CV697914	single nucleotide variant	NM_020169.4(LXN):c.143G>A (p.Arg48Lys)	not provided [RCV000951070]	benign\|likely benign	3	158671006	158671006	Human		name
156387940	CV2221667	single nucleotide variant	NM_020169.4(LXN):c.391C>G (p.Pro131Ala)	not specified [RCV004096908]	uncertain significance	3	158669112	158669112	Human		name
156005090	CV2290287	single nucleotide variant	NM_020169.4(LXN):c.560T>C (p.Ile187Thr)	not specified [RCV004152933]	uncertain significance	3	158667022	158667022	Human		name
407481080	CV3449317	single nucleotide variant	NM_020169.4(LXN):c.322C>G (p.Gln108Glu)	not specified [RCV004640302]	uncertain significance	3	158669481	158669481	Human		name
15190601	CV720278	single nucleotide variant	NM_020169.4(LXN):c.641G>A (p.Arg214His)	not provided [RCV000888145]	likely benign	3	158666674	158666674	Human	1	name
15190601	CV720278	single nucleotide variant	NM_020169.4(LXN):c.641G>A (p.Arg214His)	not provided [RCV000888145]	likely benign	3	158666674	158666675	Human	1	name
15168736	CV720280	single nucleotide variant	NM_020169.4(LXN):c.406G>A (p.Val136Ile)	not provided [RCV000883126]	benign	3	158669097	158669097	Human		name