Lst1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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11 records found for search term Lst1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598223827	CV3981151	single nucleotide variant	NM_205839.3(LST1):c.136-17T>C	not specified [RCV005380110]	likely benign	6	31588501	31588501	Human		name
597635301	CV3699573	single nucleotide variant	NM_205839.3(LST1):c.33C>T (p.Tyr11=)	not specified [RCV004940563]	likely benign	6	31587654	31587654	Human		name
598223821	CV3981150	single nucleotide variant	NM_205839.3(LST1):c.24A>G (p.Ile8Met)	not specified [RCV005380109]	uncertain significance	6	31587645	31587645	Human		name
156193017	CV2325793	single nucleotide variant	NM_205839.3(LST1):c.67G>C (p.Ala23Pro)	not specified [RCV004173680]	uncertain significance	6	31587688	31587688	Human		name
401766914	CV2680191	single nucleotide variant	NM_205839.3(LST1):c.52G>A (p.Gly18Arg)	not specified [RCV004286668]	uncertain significance	6	31587673	31587673	Human		name
401739693	CV2684144	single nucleotide variant	NM_205839.3(LST1):c.38G>A (p.Gly13Asp)	not specified [RCV004288819]	uncertain significance	6	31587659	31587659	Human		name
155962950	CV2388325	single nucleotide variant	NM_205839.3(LST1):c.247G>A (p.Asp83Asn)	not specified [RCV004234776]	uncertain significance	6	31588629	31588629	Human		name
405810911	CV3284496	single nucleotide variant	NM_205839.3(LST1):c.263A>C (p.Tyr88Ser)	not specified [RCV004408224]	uncertain significance	6	31588645	31588645	Human		name
405810913	CV3284497	single nucleotide variant	NM_205839.3(LST1):c.265G>A (p.Ala89Thr)	not specified [RCV004408225]	likely benign	6	31588647	31588647	Human		name
407468473	CV3453100	single nucleotide variant	NM_205839.3(LST1):c.226G>T (p.Asp76Tyr)	not specified [RCV004636296]	uncertain significance	6	31588608	31588608	Human		name
598252807	CV3985096	single nucleotide variant	NM_205839.3(LST1):c.106C>G (p.Arg36Gly)	not specified [RCV005366780]	likely benign	6	31587727	31587727	Human		name