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Variants search result for Homo sapiens
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46 records found for search term Znf770
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407479310CV3423556single nucleotide variantNM_014106.4(ZNF770):c.25A>G (p.Met9Val)not specified [RCV004601971]uncertain significance153498341034983410Humanname
597735942CV3639124single nucleotide variantNM_014106.4(ZNF770):c.238C>T (p.Pro80Ser)not specified [RCV004889601]uncertain significance153498319734983197Humanname
156158185CV2236074single nucleotide variantNM_014106.4(ZNF770):c.989A>G (p.Tyr330Cys)not specified [RCV004114231]uncertain significance153498244634982446Humanname
156255912CV2359501single nucleotide variantNM_014106.4(ZNF770):c.425A>G (p.His142Arg)not specified [RCV004214812]uncertain significance153498301034983010Humanname
329377829CV2460724single nucleotide variantNM_014106.4(ZNF770):c.320A>G (p.Tyr107Cys)not specified [RCV004271063]uncertain significance153498311534983115Humanname
401753108CV2674781single nucleotide variantNM_014106.4(ZNF770):c.459G>C (p.Met153Ile)not specified [RCV004294060]uncertain significance153498297634982976Humanname
401754270CV2685217single nucleotide variantNM_014106.4(ZNF770):c.734G>A (p.Arg245Gln)not specified [RCV004289772]likely benign153498270134982701Humanname
401768883CV2686414single nucleotide variantNM_014106.4(ZNF770):c.427C>G (p.Pro143Ala)not specified [RCV004297484]uncertain significance153498300834983008Humanname
401768885CV2686415single nucleotide variantNM_014106.4(ZNF770):c.452A>G (p.Tyr151Cys)not specified [RCV004297485]uncertain significance153498298334982983Humanname
401760353CV2695013single nucleotide variantNM_014106.4(ZNF770):c.311A>G (p.Asn104Ser)not specified [RCV004301387]uncertain significance153498312434983124Humanname
401764692CV2705211single nucleotide variantNM_014106.4(ZNF770):c.962A>G (p.Lys321Arg)not specified [RCV004311915]uncertain significance153498247334982473Humanname
401884655CV2755944single nucleotide variantNM_014106.4(ZNF770):c.443A>G (p.Asp148Gly)not specified [RCV004336032]uncertain significance153498299234982992Humanname
405701993CV3351393single nucleotide variantNM_014106.4(ZNF770):c.372G>C (p.Lys124Asn)not specified [RCV004492602]uncertain significance153498306334983063Humanname
405702004CV3351394single nucleotide variantNM_014106.4(ZNF770):c.542T>C (p.Ile181Thr)not specified [RCV004492603]uncertain significance153498289334982893Humanname
405702012CV3351395single nucleotide variantNM_014106.4(ZNF770):c.601A>G (p.Thr201Ala)not specified [RCV004492604]uncertain significance153498283434982834Humanname
405702022CV3351396single nucleotide variantNM_014106.4(ZNF770):c.742T>A (p.Leu248Ile)not specified [RCV004492605]uncertain significance153498269334982693Humanname
597735936CV3639123single nucleotide variantNM_014106.4(ZNF770):c.419C>T (p.Ala140Val)not specified [RCV004889600]uncertain significance153498301634983016Humanname
597735947CV3639125single nucleotide variantNM_014106.4(ZNF770):c.970A>G (p.Ser324Gly)not specified [RCV004889602]uncertain significance153498246534982465Humanname
597735952CV3639126single nucleotide variantNM_014106.4(ZNF770):c.856G>A (p.Val286Ile)not specified [RCV004889603]uncertain significance153498257934982579Humanname
597735958CV3639127single nucleotide variantNM_014106.4(ZNF770):c.733C>T (p.Arg245Trp)not specified [RCV004889604]uncertain significance153498270234982702Humanname
598186027CV3949265single nucleotide variantNM_014106.4(ZNF770):c.695T>G (p.Leu232Arg)not specified [RCV005311801]uncertain significance153498274034982740Humanname
598272188CV3949267single nucleotide variantNM_014106.4(ZNF770):c.593G>A (p.Arg198Gln)not specified [RCV005303062]uncertain significance153498284234982842Humanname
598272199CV3949270single nucleotide variantNM_014106.4(ZNF770):c.796A>G (p.Asn266Asp)not specified [RCV005303064]uncertain significance153498263934982639Humanname
156340989CV2225731single nucleotide variantNM_014106.4(ZNF770):c.1637C>T (p.Ser546Phe)not specified [RCV004103147]likely benign153498179834981798Humanname
155927862CV2227403single nucleotide variantNM_014106.4(ZNF770):c.1841C>T (p.Ser614Leu)not specified [RCV004092069]uncertain significance153498159434981594Humanname
156044273CV2237635single nucleotide variantNM_014106.4(ZNF770):c.1292T>C (p.Ile431Thr)not specified [RCV004106566]uncertain significance153498214334982143Humanname
156166458CV2243607single nucleotide variantNM_014106.4(ZNF770):c.1268T>G (p.Leu423Arg)not specified [RCV004114335]uncertain significance153498216734982167Humanname
156017588CV2262907single nucleotide variantNM_014106.4(ZNF770):c.1034G>A (p.Arg345His)not specified [RCV004125051]uncertain significance153498240134982401Humanname
156096055CV2297418single nucleotide variantNM_014106.4(ZNF770):c.1641T>A (p.Asn547Lys)not specified [RCV004153359]uncertain significance153498179434981794Humanname
156276389CV2330751single nucleotide variantNM_014106.4(ZNF770):c.1129A>T (p.Ser377Cys)not specified [RCV004185814]uncertain significance153498230634982306Humanname
156097640CV2375680single nucleotide variantNM_014106.4(ZNF770):c.1393A>G (p.Arg465Gly)not specified [RCV004226154]uncertain significance153498204234982042Humanname
329372227CV2443066single nucleotide variantNM_014106.4(ZNF770):c.1033C>T (p.Arg345Cys)not specified [RCV004253653]uncertain significance153498240234982402Humanname
329361944CV2448140single nucleotide variantNM_014106.4(ZNF770):c.1271C>T (p.Thr424Met)not specified [RCV004263358]uncertain significance153498216434982164Humanname
405701968CV3351389single nucleotide variantNM_014106.4(ZNF770):c.1247G>A (p.Gly416Glu)not specified [RCV004492598]uncertain significance153498218834982188Humanname
405701977CV3351390single nucleotide variantNM_014106.4(ZNF770):c.1610T>A (p.Val537Glu)not specified [RCV004492599]uncertain significance153498182534981825Humanname
405701982CV3351391single nucleotide variantNM_014106.4(ZNF770):c.1765C>T (p.Pro589Ser)not specified [RCV004492600]uncertain significance153498167034981670Humanname
405701989CV3351392single nucleotide variantNM_014106.4(ZNF770):c.1831T>C (p.Cys611Arg)not specified [RCV004492601]uncertain significance153498160434981604Humanname
407479293CV3423552single nucleotide variantNM_014106.4(ZNF770):c.1631A>G (p.Asn544Ser)not specified [RCV004601967]uncertain significance153498180434981804Humanname
407479301CV3423554single nucleotide variantNM_014106.4(ZNF770):c.1151C>T (p.Thr384Ile)not specified [RCV004601969]uncertain significance153498228434982284Humanname
407479305CV3423555single nucleotide variantNM_014106.4(ZNF770):c.1225C>T (p.Pro409Ser)not specified [RCV004601970]uncertain significance153498221034982210Humanname
407479314CV3423557single nucleotide variantNM_014106.4(ZNF770):c.1224G>T (p.Leu408Phe)not specified [RCV004601972]uncertain significance153498221134982211Humanname
407479318CV3423558single nucleotide variantNM_014106.4(ZNF770):c.1160G>T (p.Gly387Val)not specified [RCV004601973]uncertain significance153498227534982275Humanname
407479322CV3423559single nucleotide variantNM_014106.4(ZNF770):c.1448T>C (p.Val483Ala)not specified [RCV004601974]uncertain significance153498198734981987Humanname
597735931CV3639122single nucleotide variantNM_014106.4(ZNF770):c.1075A>G (p.Lys359Glu)not specified [RCV004889599]uncertain significance153498236034982360Humanname
598272193CV3949268single nucleotide variantNM_014106.4(ZNF770):c.1304T>G (p.Val435Gly)not specified [RCV005303063]uncertain significance153498213134982131Humanname
598186034CV3949269single nucleotide variantNM_014106.4(ZNF770):c.1244T>A (p.Met415Lys)not specified [RCV005311802]uncertain significance153498219134982191Humanname