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45 records found for search term Pdia6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
408390163CV3519229deletionNM_005742.4(PDIA6):c.831_840+13delnot provided [RCV004762538]uncertain significance21078973610789758Humanname
8576258CV110616single nucleotide variantNM_001282704.1(PDIA6):c.-54-2243A>GLung cancer [RCV000091139]uncertain significance21082316110823161Humanname
405690789CV3227443deletionNM_005742.4(PDIA6):c.286del (p.Gln96fs)not provided [RCV003991787]uncertain significance21079714110797141Humanname
405777188CV3371904single nucleotide variantNM_005742.4(PDIA6):c.64T>A (p.Ser22Thr)not specified [RCV004503343]uncertain significance21080259610802596Humanname
151349405CV1325315deletionNM_005742.4(PDIA6):c.547del (p.Val183fs)not provided [RCV001814609]uncertain significance21079183210791832Humanname
155681036CV1781420deletionNM_005742.4(PDIA6):c.702del (p.Arg235fs)See cases [RCV002306448]likely pathogenic21078988710789887Humanname
156376332CV2210544single nucleotide variantNM_005742.4(PDIA6):c.256C>T (p.His86Tyr)not specified [RCV004083357]uncertain significance21079717110797171Humanname
401750524CV2701313single nucleotide variantNM_005742.4(PDIA6):c.145G>A (p.Glu49Lys)not specified [RCV004311690]uncertain significance21080251510802515Humanname
405777141CV3375459single nucleotide variantNM_005742.4(PDIA6):c.107A>G (p.Asn36Ser)not specified [RCV004503335]uncertain significance21080255310802553Humanname
156300912CV2248893single nucleotide variantNM_005742.4(PDIA6):c.413G>A (p.Arg138His)not specified [RCV004115902]uncertain significance21079313610793136Humanname
156071478CV2254899single nucleotide variantNM_005742.4(PDIA6):c.895G>T (p.Val299Leu)not specified [RCV004117142]uncertain significance21078892710788927Humanname
156167237CV2345276single nucleotide variantNM_005742.4(PDIA6):c.821C>T (p.Pro274Leu)not specified [RCV004196011]uncertain significance21078976810789768Humanname
156185394CV2346518single nucleotide variantNM_005742.4(PDIA6):c.697G>A (p.Gly233Arg)not specified [RCV004206439]uncertain significance21079072110790721Humanname
401766327CV2679648single nucleotide variantNM_005742.4(PDIA6):c.907C>G (p.Pro303Ala)not specified [RCV004282121]uncertain significance21078891510788915Humanname
401855228CV2757190single nucleotide variantNM_005742.4(PDIA6):c.632C>T (p.Thr211Met)not specified [RCV004338794]uncertain significance21079078610790786Humanname
401864925CV2768601single nucleotide variantNM_005742.4(PDIA6):c.947A>G (p.Tyr316Cys)not specified [RCV004344460]uncertain significance21078874810788748Humanname
401866270CV2782810single nucleotide variantNM_005742.4(PDIA6):c.845T>G (p.Ile282Ser)not specified [RCV004361623]uncertain significance21078897710788977Humanname
401896706CV2791987single nucleotide variantNM_005742.4(PDIA6):c.847A>G (p.Asn283Asp)not specified [RCV004359407]uncertain significance21078897510788975Humanname
405777170CV3371901single nucleotide variantNM_005742.4(PDIA6):c.394C>T (p.Arg132Cys)not specified [RCV004503340]uncertain significance21079315510793155Humanname
405777176CV3371902single nucleotide variantNM_005742.4(PDIA6):c.425G>A (p.Arg142Gln)not specified [RCV004503341]uncertain significance21079312410793124Humanname
405777182CV3371903single nucleotide variantNM_005742.4(PDIA6):c.487A>G (p.Ile163Val)not specified [RCV004503342]uncertain significance21079189210791892Humanname
405777193CV3371905single nucleotide variantNM_005742.4(PDIA6):c.707G>A (p.Gly236Glu)not specified [RCV004503344]uncertain significance21078988210789882Humanname
405777197CV3371906single nucleotide variantNM_005742.4(PDIA6):c.719T>A (p.Ile240Asn)not specified [RCV004503345]uncertain significance21078987010789870Humanname
407528485CV3470393single nucleotide variantNM_005742.4(PDIA6):c.433G>C (p.Gly145Arg)not specified [RCV004655565]uncertain significance21079311610793116Humanname
407528487CV3470394single nucleotide variantNM_005742.4(PDIA6):c.499G>A (p.Asp167Asn)not specified [RCV004655566]uncertain significance21079188010791880Humanname
408387722CV3518964single nucleotide variantNM_005742.4(PDIA6):c.567G>A (p.Trp189Ter)not provided [RCV004761283]uncertain significance21079181210791812Humanname
597701236CV3579054single nucleotide variantNM_005742.4(PDIA6):c.619G>A (p.Val207Ile)not specified [RCV004839678]uncertain significance21079079910790799Humanname
597756841CV3579056single nucleotide variantNM_005742.4(PDIA6):c.562C>T (p.Pro188Ser)not specified [RCV004848206]uncertain significance21079181710791817Humanname
597701218CV3579057single nucleotide variantNM_005742.4(PDIA6):c.523C>G (p.Leu175Val)not specified [RCV004839680]uncertain significance21079185610791856Humanname
597701210CV3579058single nucleotide variantNM_005742.4(PDIA6):c.394C>G (p.Arg132Gly)not specified [RCV004839681]uncertain significance21079315510793155Humanname
597701194CV3579060single nucleotide variantNM_005742.4(PDIA6):c.759C>A (p.Asp253Glu)not specified [RCV004839683]uncertain significance21078983010789830Humanname
597756847CV3579061single nucleotide variantNM_005742.4(PDIA6):c.784G>T (p.Val262Leu)not specified [RCV004848207]uncertain significance21078980510789805Humanname
597701178CV3579063single nucleotide variantNM_005742.4(PDIA6):c.359G>A (p.Gly120Asp)not specified [RCV004839685]uncertain significance21079319010793190Humanname
598167103CV4002506single nucleotide variantNM_005742.4(PDIA6):c.403G>A (p.Val135Met)not specified [RCV005391629]uncertain significance21079314610793146Humanname
156050153CV2367445single nucleotide variantNM_005742.4(PDIA6):c.1229A>C (p.Glu410Ala)not specified [RCV004211388]uncertain significance21078495910784959Humanname
156183687CV2382264single nucleotide variantNM_005742.4(PDIA6):c.1042G>A (p.Ala348Thr)not specified [RCV004228205]uncertain significance21078739610787396Humanname
156197221CV2400713single nucleotide variantNM_005742.4(PDIA6):c.1198G>C (p.Gly400Arg)not specified [RCV004242382]uncertain significance21078499010784990Humanname
401783387CV2723518single nucleotide variantNM_005742.4(PDIA6):c.1219G>C (p.Val407Leu)not specified [RCV004323924]uncertain significance21078496910784969Humanname
405777147CV3371897single nucleotide variantNM_005742.4(PDIA6):c.1091C>T (p.Ala364Val)not specified [RCV004503336]uncertain significance21078734710787347Humanname
405777152CV3371898single nucleotide variantNM_005742.4(PDIA6):c.1121G>C (p.Gly374Ala)not specified [RCV004503337]uncertain significance21078731710787317Humanname
405777158CV3371899single nucleotide variantNM_005742.4(PDIA6):c.1219G>A (p.Val407Ile)not specified [RCV004503338]uncertain significance21078496910784969Humanname
597701227CV3579055single nucleotide variantNM_005742.4(PDIA6):c.1219G>T (p.Val407Phe)not specified [RCV004839679]uncertain significance21078496910784969Humanname
597701202CV3579059single nucleotide variantNM_005742.4(PDIA6):c.1004T>A (p.Leu335Gln)not specified [RCV004839682]uncertain significance21078743410787434Humanname
597701186CV3579062single nucleotide variantNM_005742.4(PDIA6):c.1262T>C (p.Val421Ala)not specified [RCV004839684]uncertain significance21078431910784319Humanname
598196334CV4002507single nucleotide variantNM_005742.4(PDIA6):c.1189C>T (p.Pro397Ser)not specified [RCV005397695]uncertain significance21078499910784999Humanname