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Variants search result for Homo sapiens
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45 records found for search term Lrch2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8587081CV121707single nucleotide variantNM_020871.3(LRCH2):c.1463+1748G>TLung cancer [RCV000102227]uncertain significanceX115161928115161928Humanname
407461301CV3446022single nucleotide variantNM_020871.4(LRCH2):c.16G>A (p.Gly6Arg)not specified [RCV004634092]uncertain significanceX115234026115234026Humanname
597623550CV3699195single nucleotide variantNM_020871.4(LRCH2):c.22G>C (p.Gly8Arg)not specified [RCV004936568]uncertain significanceX115234020115234020Humanname
401921423CV2826837single nucleotide variantNM_020871.4(LRCH2):c.312G>A (p.Pro104=)not provided [RCV003432424]likely benignX115233730115233730Humanname
156136398CV2245703single nucleotide variantNM_020871.4(LRCH2):c.100G>C (p.Gly34Arg)not specified [RCV004111580]uncertain significanceX115233942115233942Humanname
156190405CV2339579single nucleotide variantNM_020871.4(LRCH2):c.104C>G (p.Ala35Gly)not specified [RCV004194244]uncertain significanceX115233938115233938Humanname
401767460CV2729673single nucleotide variantNM_020871.4(LRCH2):c.110G>A (p.Gly37Glu)not specified [RCV004331933]uncertain significanceX115233932115233932Humanname
401921397CV2826818single nucleotide variantNM_020871.4(LRCH2):c.2250G>T (p.Ala750=)not provided [RCV003432405]likely benignX115113264115113264Humanname
401921613CV2826820single nucleotide variantNM_020871.4(LRCH2):c.1032C>G (p.Gly344=)not provided [RCV003432407]likely benignX115166309115166309Humanname
407471795CV3446018single nucleotide variantNM_020871.4(LRCH2):c.167T>C (p.Phe56Ser)not specified [RCV004637469]uncertain significanceX115233875115233875Humanname
407471799CV3446019single nucleotide variantNM_020871.4(LRCH2):c.203C>T (p.Pro68Leu)not specified [RCV004637470]uncertain significanceX115233839115233839Humanname
407471814CV3446023single nucleotide variantNM_020871.4(LRCH2):c.286A>G (p.Ser96Gly)not specified [RCV004637473]likely benignX115233756115233756Humanname
598249300CV3991993single nucleotide variantNM_020871.4(LRCH2):c.269C>G (p.Ser90Cys)not specified [RCV005366352]uncertain significanceX115233773115233773Humanname
151727142CV1334490single nucleotide variantNM_020871.4(LRCH2):c.772A>G (p.Lys258Glu)Cerebellar ataxia [RCV002051959]pathogenicX115179519115179519Human2name
155991228CV2355351single nucleotide variantNM_020871.4(LRCH2):c.364C>T (p.Arg122Cys)not specified [RCV004203199]uncertain significanceX115188356115188356Humanname
405815727CV3280466single nucleotide variantNM_020871.4(LRCH2):c.971G>A (p.Arg324Gln)not specified [RCV004410712]uncertain significanceX115170326115170326Humanname
405815728CV3280467single nucleotide variantNM_020871.4(LRCH2):c.991A>G (p.Thr331Ala)not specified [RCV004410713]uncertain significanceX115170306115170306Humanname
597623551CV3699196single nucleotide variantNM_020871.4(LRCH2):c.962T>C (p.Leu321Ser)not specified [RCV004936569]uncertain significanceX115170335115170335Humanname
156334323CV2230908single nucleotide variantNM_020871.4(LRCH2):c.2092C>T (p.Pro698Ser)not specified [RCV004092380]uncertain significanceX115122768115122768Humanname
156087053CV2241293single nucleotide variantNM_020871.4(LRCH2):c.1705A>G (p.Met569Val)not specified [RCV004102439]uncertain significanceX115130190115130190Humanname
156095216CV2253012single nucleotide variantNM_020871.4(LRCH2):c.1207G>T (p.Val403Leu)not specified [RCV004120811]uncertain significanceX115165647115165647Humanname
156031878CV2259416single nucleotide variantNM_020871.4(LRCH2):c.1517A>T (p.Glu506Val)not specified [RCV004122636]uncertain significanceX115156614115156614Humanname
156254241CV2284150single nucleotide variantNM_020871.4(LRCH2):c.1628C>T (p.Ser543Phe)not specified [RCV004144741]uncertain significanceX115149894115149894Humanname
156339752CV2367676single nucleotide variantNM_020871.4(LRCH2):c.1636A>G (p.Ile546Val)not specified [RCV004211595]uncertain significanceX115149886115149886Humanname
155994043CV2379493single nucleotide variantNM_020871.4(LRCH2):c.1322C>T (p.Ser441Phe)not specified [RCV004217209]uncertain significanceX115165438115165438Humanname
329378403CV2446998single nucleotide variantNM_020871.4(LRCH2):c.1147A>T (p.Thr383Ser)not specified [RCV004257835]uncertain significanceX115165892115165892Humanname
329396352CV2459545single nucleotide variantNM_020871.4(LRCH2):c.1109G>A (p.Ser370Asn)not specified [RCV004277002]uncertain significanceX115165930115165930Humanname
401775900CV2692530single nucleotide variantNM_020871.4(LRCH2):c.2224G>A (p.Val742Met)not specified [RCV004312278]uncertain significanceX115113290115113290Humanname
401775263CV2710496single nucleotide variantNM_020871.4(LRCH2):c.1769C>T (p.Thr590Ile)not specified [RCV004319428]uncertain significanceX115126865115126865Humanname
401760894CV2726575single nucleotide variantNM_020871.4(LRCH2):c.2074A>G (p.Ser692Gly)not specified [RCV004329069]uncertain significanceX115122786115122786Humanname
401860072CV2794461single nucleotide variantNM_020871.4(LRCH2):c.1948C>T (p.Arg650Ter)not provided [RCV003387629]uncertain significanceX115123094115123094Humanname
401921398CV2826819single nucleotide variantNM_020871.4(LRCH2):c.2053A>G (p.Ile685Val)not provided [RCV003432406]likely benignX115122807115122807Humanname
405815725CV3280464single nucleotide variantNM_020871.4(LRCH2):c.1733A>T (p.Asn578Ile)not specified [RCV004410710]uncertain significanceX115130162115130162Humanname
407471803CV3446020single nucleotide variantNM_020871.4(LRCH2):c.1111C>G (p.Leu371Val)not specified [RCV004637471]uncertain significanceX115165928115165928Humanname
407471809CV3446021single nucleotide variantNM_020871.4(LRCH2):c.1768A>G (p.Thr590Ala)not specified [RCV004637472]uncertain significanceX115126866115126866Humanname
597623547CV3699190single nucleotide variantNM_020871.4(LRCH2):c.1953A>T (p.Gln651His)not specified [RCV004936565]uncertain significanceX115123089115123089Humanname
597623548CV3699191single nucleotide variantNM_020871.4(LRCH2):c.1757C>A (p.Ala586Asp)not specified [RCV004936566]uncertain significanceX115126877115126877Humanname
597623549CV3699192single nucleotide variantNM_020871.4(LRCH2):c.1603A>G (p.Ile535Val)not specified [RCV004936567]uncertain significanceX115149919115149919Humanname
597796110CV3699194single nucleotide variantNM_020871.4(LRCH2):c.1664G>A (p.Arg555Gln)not specified [RCV004935106]uncertain significanceX115149858115149858Humanname
597796113CV3699197single nucleotide variantNM_020871.4(LRCH2):c.2096C>T (p.Ala699Val)not specified [RCV004935107]uncertain significanceX115122764115122764Humanname
598261814CV3991992single nucleotide variantNM_020871.4(LRCH2):c.1859G>A (p.Arg620His)not specified [RCV005347921]uncertain significanceX115123183115123183Humanname
598261820CV3991994single nucleotide variantNM_020871.4(LRCH2):c.1186G>T (p.Asp396Tyr)not specified [RCV005347922]uncertain significanceX115165853115165853Humanname
598249315CV3991997single nucleotide variantNM_020871.4(LRCH2):c.1679G>A (p.Arg560Lys)not specified [RCV005366355]uncertain significanceX115149843115149843Humanname
598249321CV3991998single nucleotide variantNM_020871.4(LRCH2):c.1286C>T (p.Ser429Leu)not specified [RCV005366356]uncertain significanceX115165568115165568Humanname
598231032CV3991999single nucleotide variantNM_020871.4(LRCH2):c.1616C>T (p.Pro539Leu)not specified [RCV005362801]uncertain significanceX115149906115149906Humanname