Lat2 Variant Search Result - Rat Genome Database

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25 records found for search term Lat2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401776861	CV2711445	single nucleotide variant	NM_032464.3(LAT2):c.80G>A (p.Arg27His)	not specified [RCV004306772]	uncertain significance	7	74216055	74216055	Human		name
401771166	CV2726386	single nucleotide variant	NM_032464.3(LAT2):c.38C>T (p.Ala13Val)	not specified [RCV004328601]	uncertain significance	7	74216013	74216013	Human		name
598197848	CV3987716	single nucleotide variant	NM_032464.3(LAT2):c.91C>T (p.Pro31Ser)	not specified [RCV005355412]	uncertain significance	7	74216066	74216066	Human		name
156179185	CV2201639	single nucleotide variant	NM_032464.3(LAT2):c.137G>A (p.Arg46His)	not specified [RCV004082101]	uncertain significance	7	74219746	74219746	Human		name
156311926	CV2256786	single nucleotide variant	NM_032464.3(LAT2):c.209C>T (p.Ala70Val)	not specified [RCV004121010]	likely benign	7	74219990	74219990	Human		name
401728012	CV2685738	single nucleotide variant	NM_032464.3(LAT2):c.158C>T (p.Thr53Met)	not specified [RCV004294732]	uncertain significance	7	74219767	74219767	Human		name
401733137	CV2691213	single nucleotide variant	NM_032464.3(LAT2):c.209C>A (p.Ala70Glu)	not specified [RCV004302987]	likely benign	7	74219990	74219990	Human		name
401721728	CV2710129	single nucleotide variant	NM_032464.3(LAT2):c.228G>T (p.Arg76Ser)	not specified [RCV004315180]	uncertain significance	7	74220217	74220217	Human		name
401855499	CV2757365	single nucleotide variant	NM_032464.3(LAT2):c.184G>A (p.Gly62Arg)	not specified [RCV004340767]	likely benign	7	74219965	74219965	Human		name
407482186	CV3452405	single nucleotide variant	NM_032464.3(LAT2):c.199G>C (p.Gly67Arg)	not specified [RCV004640089]	uncertain significance	7	74219980	74219980	Human		name
597795380	CV3701610	single nucleotide variant	NM_032464.3(LAT2):c.142G>A (p.Asp48Asn)	not specified [RCV004934851]	likely benign	7	74219751	74219751	Human		name
401729712	CV2690469	single nucleotide variant	NM_032464.3(LAT2):c.530G>A (p.Gly177Asp)	not specified [RCV004304237]	uncertain significance	7	74224099	74224099	Human		name
401883757	CV2754973	single nucleotide variant	NM_032464.3(LAT2):c.391G>C (p.Asp131His)	not specified [RCV004341438]	uncertain significance	7	74223726	74223726	Human		name
401886355	CV2771754	single nucleotide variant	NM_032464.3(LAT2):c.682G>A (p.Asp228Asn)	not specified [RCV004350533]	uncertain significance	7	74224692	74224692	Human		name
405815255	CV3283652	single nucleotide variant	NM_032464.3(LAT2):c.467T>C (p.Ile156Thr)	not specified [RCV004410240]	likely benign	7	74224036	74224036	Human		name
405815256	CV3283653	single nucleotide variant	NM_032464.3(LAT2):c.478T>C (p.Cys160Arg)	not specified [RCV004410241]	uncertain significance	7	74224047	74224047	Human		name
405815258	CV3283655	single nucleotide variant	NM_032464.3(LAT2):c.551C>T (p.Pro184Leu)	not specified [RCV004410243]	uncertain significance	7	74224120	74224120	Human		name
405815259	CV3283656	single nucleotide variant	NM_032464.3(LAT2):c.641G>A (p.Arg214Lys)	not specified [RCV004410244]	uncertain significance	7	74224651	74224651	Human		name
407460396	CV3452406	single nucleotide variant	NM_032464.3(LAT2):c.685G>A (p.Gly229Arg)	not specified [RCV004633881]	uncertain significance	7	74224695	74224695	Human		name
407482192	CV3452407	single nucleotide variant	NM_032464.3(LAT2):c.347T>C (p.Met116Thr)	not specified [RCV004640090]	likely benign	7	74221651	74221651	Human		name
597631638	CV3701605	single nucleotide variant	NM_032464.3(LAT2):c.647C>T (p.Ala216Val)	not specified [RCV004939826]	uncertain significance	7	74224657	74224657	Human		name
597631641	CV3701606	single nucleotide variant	NM_032464.3(LAT2):c.692C>T (p.Pro231Leu)	not specified [RCV004939827]	uncertain significance	7	74224702	74224702	Human		name
597631645	CV3701607	single nucleotide variant	NM_032464.3(LAT2):c.374C>T (p.Ser125Leu)	not specified [RCV004939828]	uncertain significance	7	74221678	74221678	Human		name
597631647	CV3701608	single nucleotide variant	NM_032464.3(LAT2):c.391G>A (p.Asp131Asn)	not specified [RCV004939829]	uncertain significance	7	74223726	74223726	Human		name
598174767	CV3987715	single nucleotide variant	NM_032464.3(LAT2):c.602A>G (p.Gln201Arg)	not specified [RCV005371168]	uncertain significance	7	74224171	74224171	Human		name

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