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Variants search result for Homo sapiens
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40 records found for search term Lrrtm3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405810626CV3284353single nucleotide variantNM_178011.5(LRRTM3):c.23T>C (p.Leu8Pro)not specified [RCV004408081]uncertain significance106692693966926939Humanname
8633693CV88908single nucleotide variantNM_178011.4(LRRTM3):c.285C>T (p.Asn95=)Malignant melanoma [RCV000069003]not provided106692720166927201Humanname
407475871CV3415824single nucleotide variantNM_178011.5(LRRTM3):c.660C>T (p.Leu220=)not provided [RCV004598701]likely benign106692757666927576Humanname
597634633CV3702462single nucleotide variantNM_178011.5(LRRTM3):c.61A>G (p.Thr21Ala)not specified [RCV004940460]uncertain significance106692697766926977Humanname
598253016CV3985027single nucleotide variantNM_178011.5(LRRTM3):c.91G>C (p.Glu31Gln)not specified [RCV005366747]uncertain significance106692700766927007Humanname
8657448CV88907single nucleotide variantNM_178011.4(LRRTM3):c.95G>A (p.Arg32Gln)Malignant melanoma [RCV000069002]not provided106692701166927011Humanname
329391633CV2452991single nucleotide variantNM_178011.5(LRRTM3):c.166C>A (p.Pro56Thr)not specified [RCV004277615]uncertain significance106692708266927082Humanname
408378264CV3500929single nucleotide variantNM_178011.5(LRRTM3):c.1278G>T (p.Ala426=)not provided [RCV004722579]likely benign106692819466928194Humanname
597634622CV3702460single nucleotide variantNM_178011.5(LRRTM3):c.231G>C (p.Lys77Asn)not specified [RCV004940458]uncertain significance106692714766927147Humanname
597634627CV3702461single nucleotide variantNM_178011.5(LRRTM3):c.109G>T (p.Gly37Cys)not specified [RCV004940459]uncertain significance106692702566927025Humanname
597634648CV3702465single nucleotide variantNM_178011.5(LRRTM3):c.255C>A (p.Asn85Lys)not specified [RCV004940463]uncertain significance106692717166927171Humanname
8657449CV88909single nucleotide variantNM_178011.4(LRRTM3):c.1650G>A (p.Gln550=)Malignant melanoma [RCV000069004]not provided106709770067097700Humanname
156233731CV2274008single nucleotide variantNM_178011.5(LRRTM3):c.383C>T (p.Thr128Ile)not specified [RCV004134396]uncertain significance106692729966927299Humanname
156176501CV2327107single nucleotide variantNM_178011.5(LRRTM3):c.668C>T (p.Ala223Val)not specified [RCV004178678]uncertain significance106692758466927584Humanname
155985786CV2368160single nucleotide variantNM_178011.5(LRRTM3):c.436C>T (p.His146Tyr)not specified [RCV004216505]uncertain significance106692735266927352Humanname
156342829CV2368629single nucleotide variantNM_178011.5(LRRTM3):c.845G>T (p.Arg282Leu)not specified [RCV004221407]uncertain significance106692776166927761Humanname
597634642CV3702464single nucleotide variantNM_178011.5(LRRTM3):c.325C>T (p.Arg109Cys)not specified [RCV004940462]uncertain significance106692724166927241Humanname
598253022CV3985026single nucleotide variantNM_178011.5(LRRTM3):c.965C>T (p.Ser322Phe)not specified [RCV005366746]uncertain significance106692788166927881Humanname
156326971CV2217182single nucleotide variantNM_178011.5(LRRTM3):c.1250T>C (p.Phe417Ser)not specified [RCV004087638]uncertain significance106692816666928166Humanname
155934141CV2229092single nucleotide variantNM_178011.5(LRRTM3):c.1187C>T (p.Pro396Leu)not specified [RCV004098862]uncertain significance106692810366928103Humanname
156173867CV2290191single nucleotide variantNM_178011.5(LRRTM3):c.1178C>T (p.Pro393Leu)not specified [RCV004152849]uncertain significance106692809466928094Humanname
156278399CV2297420single nucleotide variantNM_178011.5(LRRTM3):c.1273G>A (p.Val425Met)not specified [RCV004153361]uncertain significance106692818966928189Humanname
329361117CV2436686single nucleotide variantNM_178011.5(LRRTM3):c.1201G>T (p.Ala401Ser)not specified [RCV004258058]uncertain significance106692811766928117Humanname
401765984CV2717965single nucleotide variantNM_178011.5(LRRTM3):c.1658C>T (p.Thr553Met)not specified [RCV004321915]uncertain significance106709770867097708Humanname
401761282CV2726701single nucleotide variantNM_178011.5(LRRTM3):c.1669C>T (p.His557Tyr)not specified [RCV004323037]uncertain significance106709771967097719Humanname
401881695CV2783925single nucleotide variantNM_178011.5(LRRTM3):c.1528G>A (p.Glu510Lys)not specified [RCV004362349]uncertain significance106692844466928444Humanname
405810620CV3284350single nucleotide variantNM_178011.5(LRRTM3):c.1189C>A (p.Pro397Thr)not specified [RCV004408078]uncertain significance106692810566928105Humanname
405810622CV3284351single nucleotide variantNM_178011.5(LRRTM3):c.1239G>T (p.Glu413Asp)not specified [RCV004408079]uncertain significance106692815566928155Humanname
405810624CV3284352single nucleotide variantNM_178011.5(LRRTM3):c.1715G>A (p.Arg572Gln)not specified [RCV004408080]uncertain significance106709776567097765Humanname
407480986CV3453028single nucleotide variantNM_178011.5(LRRTM3):c.1640C>T (p.Thr547Met)not specified [RCV004640127]uncertain significance106709769067097690Humanname
407480482CV3453029single nucleotide variantNM_178011.5(LRRTM3):c.1114G>T (p.Ala372Ser)not specified [RCV004636277]uncertain significance106692803066928030Humanname
407480991CV3453030single nucleotide variantNM_178011.5(LRRTM3):c.1181C>T (p.Pro394Leu)not specified [RCV004640128]uncertain significance106692809766928097Humanname
597634610CV3702458single nucleotide variantNM_178011.5(LRRTM3):c.1085G>A (p.Gly362Asp)not specified [RCV004940456]uncertain significance106692800166928001Humanname
597634616CV3702459single nucleotide variantNM_178011.5(LRRTM3):c.1220A>T (p.Glu407Val)not specified [RCV004940457]uncertain significance106692813666928136Humanname
597634638CV3702463single nucleotide variantNM_178011.5(LRRTM3):c.1741G>A (p.Ala581Thr)not specified [RCV004940461]uncertain significance106709779167097791Humanname
597634653CV3702466single nucleotide variantNM_178011.5(LRRTM3):c.1171A>G (p.Ser391Gly)not specified [RCV004940464]uncertain significance106692808766928087Humanname
597634659CV3702467single nucleotide variantNM_178011.5(LRRTM3):c.1057G>C (p.Asp353His)not specified [RCV004940465]uncertain significance106692797366927973Humanname
598223565CV3985023single nucleotide variantNM_178011.5(LRRTM3):c.1379G>A (p.Arg460Lys)not specified [RCV005380069]uncertain significance106692829566928295Humanname
598223576CV3985025single nucleotide variantNM_178011.5(LRRTM3):c.1306C>A (p.Leu436Met)not specified [RCV005380071]uncertain significance106692822266928222Humanname
8626839CV81983single nucleotide variantNM_178011.4(LRRTM3):c.1582C>A (p.Pro528Thr)Malignant melanoma [RCV000062062]not provided106709763267097632Humanname