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76 records found for search term Gramd1a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329367646CV2456970single nucleotide variantNM_020895.5(GRAMD1A):c.25G>T (p.Gly9Cys)not specified [RCV004270909]uncertain significance193500913535009135Humanname
405756559CV3252390single nucleotide variantNM_020895.5(GRAMD1A):c.26G>A (p.Gly9Asp)not specified [RCV004393546]uncertain significance193500913635009136Humanname
156284704CV2232734single nucleotide variantNM_020895.5(GRAMD1A):c.88C>T (p.Arg30Trp)not specified [RCV004101388]uncertain significance193500919835009198Humanname
156167376CV2330190single nucleotide variantNM_020895.5(GRAMD1A):c.53C>T (p.Ser18Leu)not specified [RCV004185675]uncertain significance193500916335009163Humanname
598187172CV3967557single nucleotide variantNM_020895.5(GRAMD1A):c.59G>A (p.Arg20Gln)not specified [RCV005353645]uncertain significance193500916935009169Humanname
156132450CV2206606single nucleotide variantNM_020895.5(GRAMD1A):c.121G>A (p.Val41Met)not specified [RCV004080948]uncertain significance193500923135009231Humanname
401720954CV2702205single nucleotide variantNM_020895.5(GRAMD1A):c.183G>C (p.Gln61His)not specified [RCV004314551]uncertain significance193500929335009293Humanname
401897030CV2785516single nucleotide variantNM_020895.5(GRAMD1A):c.208C>T (p.Arg70Cys)not specified [RCV004363041]uncertain significance193500931835009318Humanname
405756545CV3252388single nucleotide variantNM_020895.5(GRAMD1A):c.197G>A (p.Arg66Gln)not specified [RCV004393544]uncertain significance193500930735009307Humanname
407527023CV3436931single nucleotide variantNM_020895.5(GRAMD1A):c.164C>G (p.Pro55Arg)not specified [RCV004632659]uncertain significance193500927435009274Humanname
156313713CV2196541single nucleotide variantNM_020895.5(GRAMD1A):c.476C>T (p.Thr159Met)not specified [RCV004073829]uncertain significance193501033035010330Humanname
156294163CV2336694single nucleotide variantNM_020895.5(GRAMD1A):c.770C>T (p.Ser257Leu)not specified [RCV004196934]uncertain significance193501359135013591Humanname
156213166CV2385831single nucleotide variantNM_020895.5(GRAMD1A):c.489C>G (p.Ile163Met)not specified [RCV004226880]uncertain significance193501034335010343Humanname
156254332CV2397539single nucleotide variantNM_020895.5(GRAMD1A):c.938C>T (p.Pro313Leu)not specified [RCV004237003]uncertain significance193501425635014256Humanname
329382566CV2424485single nucleotide variantNM_020895.5(GRAMD1A):c.619C>T (p.Arg207Cys)not specified [RCV004252374]uncertain significance193501326835013268Humanname
329392646CV2439089single nucleotide variantNM_020895.5(GRAMD1A):c.856G>A (p.Asp286Asn)not specified [RCV004266377]uncertain significance193501367735013677Humanname
329389172CV2448629single nucleotide variantNM_020895.5(GRAMD1A):c.722C>G (p.Thr241Ser)not specified [RCV004259299]likely benign193501354335013543Humanname
401750255CV2715565single nucleotide variantNM_020895.5(GRAMD1A):c.556C>T (p.Arg186Cys)not specified [RCV004326960]uncertain significance193501150435011504Humanname
401879051CV2754742single nucleotide variantNM_020895.5(GRAMD1A):c.848C>T (p.Ala283Val)not specified [RCV004341231]uncertain significance193501366935013669Humanname
401869401CV2772388single nucleotide variantNM_020895.5(GRAMD1A):c.970C>G (p.Gln324Glu)not specified [RCV004355185]uncertain significance193501428835014288Humanname
401899203CV2786009single nucleotide variantNM_020895.5(GRAMD1A):c.713G>A (p.Gly238Asp)not specified [RCV004359843]uncertain significance193501336235013362Humanname
401937194CV2808509single nucleotide variantNM_020895.5(GRAMD1A):c.785G>A (p.Arg262His)not provided [RCV003415191]likely benign193501360635013606Humanname
405756570CV3252392single nucleotide variantNM_020895.5(GRAMD1A):c.652G>A (p.Gly218Ser)not specified [RCV004393548]uncertain significance193501330135013301Humanname
405756577CV3252393single nucleotide variantNM_020895.5(GRAMD1A):c.701T>C (p.Leu234Ser)not specified [RCV004393549]uncertain significance193501335035013350Humanname
405756584CV3252394single nucleotide variantNM_020895.5(GRAMD1A):c.836A>G (p.Asn279Ser)not specified [RCV004393550]uncertain significance193501365735013657Humanname
407527017CV3436929single nucleotide variantNM_020895.5(GRAMD1A):c.968C>T (p.Thr323Ile)not specified [RCV004632657]uncertain significance193501428635014286Humanname
597746021CV3681879single nucleotide variantNM_020895.5(GRAMD1A):c.346C>T (p.Arg116Cys)not specified [RCV004922612]uncertain significance193501011235010112Humanname
597746026CV3681880single nucleotide variantNM_020895.5(GRAMD1A):c.326A>T (p.Asp109Val)not specified [RCV004922613]uncertain significance193501009235010092Humanname
597770226CV3681881single nucleotide variantNM_020895.5(GRAMD1A):c.920C>A (p.Ser307Tyr)not specified [RCV004928262]uncertain significance193501423835014238Humanname
597746030CV3681882single nucleotide variantNM_020895.5(GRAMD1A):c.794A>T (p.Glu265Val)not specified [RCV004922614]uncertain significance193501361535013615Humanname
598187148CV3967554single nucleotide variantNM_020895.5(GRAMD1A):c.988A>G (p.Thr330Ala)not specified [RCV005353642]uncertain significance193501430635014306Humanname
156083336CV2205506single nucleotide variantNM_020895.5(GRAMD1A):c.2152C>T (p.Arg718Trp)not specified [RCV004082441]uncertain significance193502611835026118Humanname
156282134CV2220711single nucleotide variantNM_020895.5(GRAMD1A):c.2026G>A (p.Val676Met)not specified [RCV004097883]uncertain significance193502349135023491Humanname
155945241CV2237956single nucleotide variantNM_020895.5(GRAMD1A):c.1526C>T (p.Ser509Leu)not specified [RCV004110997]uncertain significance193502155235021552Humanname
156086463CV2241239single nucleotide variantNM_020895.5(GRAMD1A):c.1948G>T (p.Ala650Ser)not specified [RCV004102397]uncertain significance193502333035023330Humanname
156153557CV2242106single nucleotide variantNM_020895.5(GRAMD1A):c.1546T>G (p.Trp516Gly)not specified [RCV004109327]uncertain significance193502157235021572Humanname
156160378CV2262662single nucleotide variantNM_020895.5(GRAMD1A):c.2083A>G (p.Met695Val)not specified [RCV004130857]uncertain significance193502604935026049Humanname
156053371CV2320376single nucleotide variantNM_020895.5(GRAMD1A):c.1074C>G (p.Asp358Glu)not specified [RCV004178537]uncertain significance193501582835015828Humanname
156241958CV2346963single nucleotide variantNM_020895.5(GRAMD1A):c.1166C>T (p.Ser389Leu)not specified [RCV004202408]uncertain significance193501592035015920Humanname
156189024CV2356560single nucleotide variantNM_020895.5(GRAMD1A):c.1360G>A (p.Gly454Ser)not specified [RCV004201930]uncertain significance193501941835019418Humanname
329361101CV2436673single nucleotide variantNM_020895.5(GRAMD1A):c.1660C>T (p.Arg554Trp)not specified [RCV004258045]uncertain significance193502177135021771Humanname
329353757CV2439559single nucleotide variantNM_020895.5(GRAMD1A):c.1685G>A (p.Arg562Gln)not specified [RCV004255582]uncertain significance193502179635021796Humanname
329372005CV2442983single nucleotide variantNM_020895.5(GRAMD1A):c.1456C>T (p.Arg486Trp)not specified [RCV004253576]uncertain significance193501951435019514Humanname
329351709CV2459307single nucleotide variantNM_020895.5(GRAMD1A):c.1004A>G (p.Asp335Gly)not specified [RCV004274727]uncertain significance193501432235014322Humanname
401758083CV2704162single nucleotide variantNM_020895.5(GRAMD1A):c.1970C>T (p.Pro657Leu)not specified [RCV004311175]uncertain significance193502343535023435Humanname
401772593CV2712813single nucleotide variantNM_020895.5(GRAMD1A):c.1492C>T (p.Arg498Cys)not specified [RCV004314235]uncertain significance193502151835021518Humanname
401780570CV2727450single nucleotide variantNM_020895.5(GRAMD1A):c.1552G>A (p.Gly518Ser)not specified [RCV004329656]uncertain significance193502157835021578Humanname
401864274CV2767587single nucleotide variantNM_020895.5(GRAMD1A):c.1732C>T (p.Arg578Trp)not specified [RCV004343734]uncertain significance193502184335021843Humanname
401894013CV2770224single nucleotide variantNM_020895.5(GRAMD1A):c.1274A>G (p.Tyr425Cys)not specified [RCV004356114]uncertain significance193501925135019251Humanname
405756478CV3252378single nucleotide variantNM_020895.5(GRAMD1A):c.1095C>A (p.Asp365Glu)not specified [RCV004393534]uncertain significance193501584935015849Humanname
405756487CV3252379single nucleotide variantNM_020895.5(GRAMD1A):c.1144C>T (p.Arg382Trp)not specified [RCV004393535]uncertain significance193501589835015898Humanname
405756495CV3252380single nucleotide variantNM_020895.5(GRAMD1A):c.1220C>T (p.Thr407Met)not specified [RCV004393536]uncertain significance193501919735019197Humanname
405756498CV3252381single nucleotide variantNM_020895.5(GRAMD1A):c.1313C>T (p.Ala438Val)not specified [RCV004393537]uncertain significance193501929035019290Humanname
405756505CV3252382single nucleotide variantNM_020895.5(GRAMD1A):c.1499G>A (p.Arg500Gln)not specified [RCV004393538]uncertain significance193502152535021525Humanname
405756515CV3252383single nucleotide variantNM_020895.5(GRAMD1A):c.1624G>A (p.Gly542Arg)not specified [RCV004393539]uncertain significance193502173535021735Humanname
405756520CV3252384single nucleotide variantNM_020895.5(GRAMD1A):c.1724C>A (p.Pro575His)not specified [RCV004393540]uncertain significance193502183535021835Humanname
405756528CV3252385single nucleotide variantNM_020895.5(GRAMD1A):c.1861A>G (p.Ile621Val)not specified [RCV004393541]likely benign193502324335023243Humanname
405756535CV3252386single nucleotide variantNM_020895.5(GRAMD1A):c.1911A>C (p.Glu637Asp)not specified [RCV004393542]uncertain significance193502329335023293Humanname
405756541CV3252387single nucleotide variantNM_020895.5(GRAMD1A):c.1941C>G (p.His647Gln)not specified [RCV004393543]uncertain significance193502332335023323Humanname
405756552CV3252389single nucleotide variantNM_020895.5(GRAMD1A):c.2065G>A (p.Val689Met)not specified [RCV004393545]uncertain significance193502353035023530Humanname
407504232CV3436928single nucleotide variantNM_020895.5(GRAMD1A):c.1651G>A (p.Gly551Ser)not specified [RCV004624018]uncertain significance193502176235021762Humanname
407527020CV3436930single nucleotide variantNM_020895.5(GRAMD1A):c.1007T>C (p.Leu336Pro)not specified [RCV004632658]uncertain significance193501432535014325Humanname
407527026CV3436932single nucleotide variantNM_020895.5(GRAMD1A):c.1391C>T (p.Thr464Met)not specified [RCV004632660]uncertain significance193501944935019449Humanname
407527028CV3436933single nucleotide variantNM_020895.5(GRAMD1A):c.2003C>T (p.Ala668Val)not specified [RCV004632661]uncertain significance193502346835023468Humanname
597746006CV3681874single nucleotide variantNM_020895.5(GRAMD1A):c.1768C>T (p.Arg590Cys)not specified [RCV004922609]uncertain significance193502196535021965Humanname
597770217CV3681875single nucleotide variantNM_020895.5(GRAMD1A):c.1345C>T (p.Arg449Cys)not specified [RCV004928260]uncertain significance193501940335019403Humanname
597746016CV3681878single nucleotide variantNM_020895.5(GRAMD1A):c.1468C>T (p.Arg490Trp)not specified [RCV004922611]uncertain significance193501952635019526Humanname
597770231CV3681883single nucleotide variantNM_020895.5(GRAMD1A):c.1688C>A (p.Ala563Asp)not specified [RCV004928263]uncertain significance193502179935021799Humanname
597746034CV3681884single nucleotide variantNM_020895.5(GRAMD1A):c.1138G>A (p.Ala380Thr)not specified [RCV004922615]uncertain significance193501589235015892Humanname
597770236CV3681885single nucleotide variantNM_020895.5(GRAMD1A):c.1672C>T (p.Pro558Ser)not specified [RCV004928264]uncertain significance193502178335021783Humanname
597770240CV3681886single nucleotide variantNM_020895.5(GRAMD1A):c.1185G>C (p.Gln395His)not specified [RCV004928265]uncertain significance193501593935015939Humanname
598187127CV3967551single nucleotide variantNM_020895.5(GRAMD1A):c.1258C>T (p.Arg420Cys)not specified [RCV005353639]uncertain significance193501923535019235Humanname
598187133CV3967552single nucleotide variantNM_020895.5(GRAMD1A):c.1924A>G (p.Thr642Ala)not specified [RCV005353640]uncertain significance193502330635023306Humanname
598187142CV3967553single nucleotide variantNM_020895.5(GRAMD1A):c.1145G>A (p.Arg382Gln)not specified [RCV005353641]uncertain significance193501589935015899Humanname
598187156CV3967555single nucleotide variantNM_020895.5(GRAMD1A):c.1798C>A (p.Pro600Thr)not specified [RCV005353643]uncertain significance193502199535021995Humanname
598187164CV3967556single nucleotide variantNM_020895.5(GRAMD1A):c.1334C>T (p.Thr445Met)not specified [RCV005353644]uncertain significance193501939235019392Humanname