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46 records found for search term Spag6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405275777CV3199476single nucleotide variantNM_012443.4(SPAG6):c.122-4031A>CSPAG6-related disorder [RCV003916879]likely benign102236082222360822Humanname , trait , alternate_id
15200419CV723882single nucleotide variantNM_012443.4(SPAG6):c.534G>A (p.Glu178=)not provided [RCV000890906]benign102238681522386815Humanname
329361426CV2459679single nucleotide variantNM_012443.4(SPAG6):c.167C>G (p.Thr56Arg)not specified [RCV004277106]uncertain significance102236489822364898Humanname
401894703CV2785205single nucleotide variantNM_012443.4(SPAG6):c.105G>C (p.Glu35Asp)not specified [RCV004356982]uncertain significance102234580222345802Humanname
597757158CV3600732single nucleotide variantNM_012443.4(SPAG6):c.289C>T (p.Arg97Cys)not specified [RCV004868571]uncertain significance102236849522368495Humanname
597757163CV3600733single nucleotide variantNM_012443.4(SPAG6):c.219T>A (p.Asp73Glu)not specified [RCV004868572]uncertain significance102236495022364950Humanname
617151290CV4021758single nucleotide variantNM_012443.4(SPAG6):c.1344A>C (p.Arg448=)not provided [RCV005426719]likely benign102241106022411060Humanname
15183360CV723883single nucleotide variantNM_012443.4(SPAG6):c.1035A>G (p.Ser345=)not provided [RCV000886209]likely benign102239175822391758Humanname
156400916CV2217446single nucleotide variantNM_012443.4(SPAG6):c.557T>C (p.Ile186Thr)not specified [RCV004087870]uncertain significance102238683822386838Humanname
155952262CV2306053single nucleotide variantNM_012443.4(SPAG6):c.700A>T (p.Ser234Cys)not specified [RCV004161031]uncertain significance102238784422387844Humanname
156348158CV2312649single nucleotide variantNM_012443.4(SPAG6):c.998T>C (p.Ile333Thr)not specified [RCV004169384]uncertain significance102238930522389305Humanname
156329776CV2342456single nucleotide variantNM_012443.4(SPAG6):c.913T>A (p.Cys305Ser)not specified [RCV004194060]uncertain significance102238922022389220Humanname
155937450CV2373604single nucleotide variantNM_012443.4(SPAG6):c.441G>C (p.Trp147Cys)not specified [RCV004222696]uncertain significance102236864722368647Humanname
156388369CV2380346single nucleotide variantNM_012443.4(SPAG6):c.457G>A (p.Ala153Thr)not specified [RCV004217960]uncertain significance102236866322368663Humanname
401772761CV2687805single nucleotide variantNM_012443.4(SPAG6):c.982G>A (p.Ala328Thr)not specified [RCV004302785]uncertain significance102238928922389289Humanname
401738609CV2721928single nucleotide variantNM_012443.4(SPAG6):c.850G>A (p.Glu284Lys)not specified [RCV004326428]uncertain significance102238799422387994Humanname
405788225CV3329972single nucleotide variantNM_012443.4(SPAG6):c.661C>A (p.Pro221Thr)not specified [RCV004459999]uncertain significance102238694222386942Humanname
405788229CV3329973single nucleotide variantNM_012443.4(SPAG6):c.763G>C (p.Val255Leu)not specified [RCV004460000]uncertain significance102238790722387907Humanname
405788234CV3329974single nucleotide variantNM_012443.4(SPAG6):c.928C>T (p.Arg310Trp)not specified [RCV004460001]uncertain significance102238923522389235Humanname
405788239CV3329975single nucleotide variantNM_012443.4(SPAG6):c.929G>T (p.Arg310Leu)not specified [RCV004460002]uncertain significance102238923622389236Humanname
407510476CV3481372single nucleotide variantNM_012443.4(SPAG6):c.581T>C (p.Ile194Thr)not specified [RCV004672746]uncertain significance102238686222386862Humanname
407510484CV3481375single nucleotide variantNM_012443.4(SPAG6):c.568G>A (p.Ala190Thr)not specified [RCV004672748]uncertain significance102238684922386849Humanname
407510487CV3481376single nucleotide variantNM_012443.4(SPAG6):c.583G>T (p.Ala195Ser)not specified [RCV004672749]likely benign102238686422386864Humanname
407510491CV3481377single nucleotide variantNM_012443.4(SPAG6):c.958G>A (p.Val320Ile)not specified [RCV004672750]uncertain significance102238926522389265Humanname
597757147CV3600730single nucleotide variantNM_012443.4(SPAG6):c.299A>G (p.Lys100Arg)not specified [RCV004868569]uncertain significance102236850522368505Humanname
597757168CV3600735single nucleotide variantNM_012443.4(SPAG6):c.721G>A (p.Val241Met)not specified [RCV004868573]uncertain significance102238786522387865Humanname
597757174CV3600736single nucleotide variantNM_012443.4(SPAG6):c.361A>G (p.Ile121Val)not specified [RCV004868574]uncertain significance102236856722368567Humanname
598248460CV3922602single nucleotide variantNM_012443.4(SPAG6):c.943A>G (p.Met315Val)not specified [RCV005277447]uncertain significance102238925022389250Humanname
598248475CV3922604single nucleotide variantNM_012443.4(SPAG6):c.304G>T (p.Ala102Ser)not specified [RCV005277449]uncertain significance102236851022368510Humanname
598248482CV3922605single nucleotide variantNM_012443.4(SPAG6):c.902G>A (p.Cys301Tyr)not specified [RCV005277450]uncertain significance102238920922389209Humanname
8633579CV88794single nucleotide variantNM_012443.3(SPAG6):c.815C>T (p.Ser272Phe)Malignant melanoma [RCV000068889]not provided102238795922387959Humanname
155922037CV2284255single nucleotide variantNM_012443.4(SPAG6):c.1163T>C (p.Met388Thr)not specified [RCV004146615]uncertain significance102239188622391886Humanname
155916470CV2336155single nucleotide variantNM_012443.4(SPAG6):c.1232G>A (p.Cys411Tyr)not specified [RCV004189747]uncertain significance102240119522401195Humanname
156392887CV2385443single nucleotide variantNM_012443.4(SPAG6):c.1400G>T (p.Gly467Val)not specified [RCV004233096]uncertain significance102241111622411116Humanname
329351654CV2459231single nucleotide variantNM_012443.4(SPAG6):c.1355C>T (p.Thr452Ile)not specified [RCV004274670]uncertain significance102241107122411071Humanname
401749532CV2710793single nucleotide variantNM_012443.4(SPAG6):c.1345C>T (p.Leu449Phe)not specified [RCV004308722]uncertain significance102241106122411061Humanname
405788220CV3329971single nucleotide variantNM_012443.4(SPAG6):c.1250T>G (p.Leu417Arg)not specified [RCV004459998]uncertain significance102240121322401213Humanname
407510469CV3481370single nucleotide variantNM_012443.4(SPAG6):c.1210A>G (p.Ile404Val)not specified [RCV004672744]uncertain significance102240117322401173Humanname
407510473CV3481371single nucleotide variantNM_012443.4(SPAG6):c.1041A>T (p.Glu347Asp)not specified [RCV004672745]uncertain significance102239176422391764Humanname
407510480CV3481373single nucleotide variantNM_012443.4(SPAG6):c.1343G>A (p.Arg448Gln)not specified [RCV004672747]uncertain significance102241105922411059Humanname
407525445CV3481374single nucleotide variantNM_012443.4(SPAG6):c.1402T>C (p.Ser468Pro)not specified [RCV004679261]uncertain significance102241111822411118Humanname
407510494CV3481378single nucleotide variantNM_012443.4(SPAG6):c.1180G>C (p.Glu394Gln)not specified [RCV004672751]uncertain significance102239190322391903Humanname
597757152CV3600731single nucleotide variantNM_012443.4(SPAG6):c.1310G>T (p.Ser437Ile)not specified [RCV004868570]uncertain significance102240127322401273Humanname
597741998CV3600734single nucleotide variantNM_012443.4(SPAG6):c.1047A>T (p.Glu349Asp)not specified [RCV004864987]uncertain significance102239177022391770Humanname
597757179CV3600737single nucleotide variantNM_012443.4(SPAG6):c.1172A>G (p.Glu391Gly)not specified [RCV004868575]uncertain significance102239189522391895Humanname
598248467CV3922603single nucleotide variantNM_012443.4(SPAG6):c.1427G>A (p.Ser476Asn)not specified [RCV005277448]uncertain significance102241114322411143Humanname