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60 records found for search term Acss1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8586398CV121000single nucleotide variantNM_001252675.1(ACSS1):c.*1255G>TLung cancer [RCV000101520]uncertain significance202500650725006507Humanname
401930381CV2827143single nucleotide variantNM_032501.4(ACSS1):c.432-1425C>Tnot provided [RCV003440364]likely benign202503238325032383Humanname
405773981CV3296216single nucleotide variantNM_032501.4(ACSS1):c.88G>C (p.Gly30Arg)not specified [RCV004435781]uncertain significance202505801525058015Humanname
405774021CV3296223single nucleotide variantNM_032501.4(ACSS1):c.96C>A (p.Ser32Arg)not specified [RCV004435788]uncertain significance202505800725058007Humanname
407475858CV3421703single nucleotide variantNM_032501.4(ACSS1):c.80C>T (p.Pro27Leu)not specified [RCV004600954]uncertain significance202505802325058023Humanname
401919697CV2827142single nucleotide variantNM_032501.4(ACSS1):c.1209G>A (p.Lys403=)not provided [RCV003431282]benign202502004725020047Human1name
401919697CV2827142single nucleotide variantNM_032501.4(ACSS1):c.1209G>A (p.Lys403=)not provided [RCV003431282]benign202502004725020048Human1name
405773570CV3296149single nucleotide variantNM_032501.4(ACSS1):c.132C>A (p.Ser44Arg)not specified [RCV004435714]uncertain significance202505797125057971Humanname
407501252CV3421734single nucleotide variantNM_032501.4(ACSS1):c.199C>T (p.Arg67Trp)not specified [RCV004607337]uncertain significance202505790425057904Humanname
597792672CV3647327single nucleotide variantNM_032501.4(ACSS1):c.110C>A (p.Ala37Glu)not specified [RCV004902742]uncertain significance202505799325057993Humanname
598173996CV3938950single nucleotide variantNM_032501.4(ACSS1):c.101C>A (p.Pro34Gln)not specified [RCV005309641]uncertain significance202505800225058002Humanname
156379472CV2217887single nucleotide variantNM_032501.4(ACSS1):c.661C>G (p.Gln221Glu)not specified [RCV004086351]uncertain significance202502361225023612Humanname
155915171CV2264951single nucleotide variantNM_032501.4(ACSS1):c.797C>T (p.Pro266Leu)not specified [RCV004134685]uncertain significance202502347625023476Humanname
155957866CV2282121single nucleotide variantNM_032501.4(ACSS1):c.733G>A (p.Val245Met)not specified [RCV004138857]uncertain significance202502354025023540Humanname
156083602CV2381899single nucleotide variantNM_032501.4(ACSS1):c.520G>A (p.Val174Met)not specified [RCV004225840]uncertain significance202503087025030870Humanname
156182591CV2382138single nucleotide variantNM_032501.4(ACSS1):c.946G>A (p.Ala316Thr)not specified [RCV004228097]uncertain significance202502295425022954Humanname
155902987CV2386396single nucleotide variantNM_032501.4(ACSS1):c.376G>A (p.Val126Ile)not specified [RCV004228727]likely benign202504814025048140Humanname
401740008CV2683232single nucleotide variantNM_032501.4(ACSS1):c.394C>T (p.Arg132Cys)not specified [RCV004286227]uncertain significance202504812225048122Humanname
401897450CV2787055single nucleotide variantNM_032501.4(ACSS1):c.434A>G (p.Glu145Gly)not specified [RCV004366171]uncertain significance202503095625030956Humanname
405773879CV3296200single nucleotide variantNM_032501.4(ACSS1):c.580G>A (p.Val194Ile)not specified [RCV004435765]uncertain significance202503081025030810Humanname
405773957CV3296212single nucleotide variantNM_032501.4(ACSS1):c.835G>A (p.Ala279Thr)not specified [RCV004435777]uncertain significance202502306525023065Humanname
407475822CV3421695single nucleotide variantNM_032501.4(ACSS1):c.481G>A (p.Gly161Arg)not specified [RCV004600947]uncertain significance202503090925030909Humanname
407476036CV3421745single nucleotide variantNM_032501.4(ACSS1):c.490C>T (p.Arg164Cys)not specified [RCV004600990]uncertain significance202503090025030900Humanname
597792589CV3647268single nucleotide variantNM_032501.4(ACSS1):c.805C>G (p.Gln269Glu)not specified [RCV004902689]uncertain significance202502346825023468Humanname
597792610CV3647276single nucleotide variantNM_032501.4(ACSS1):c.542C>G (p.Ala181Gly)not specified [RCV004902696]uncertain significance202503084825030848Humanname
597792817CV3647294single nucleotide variantNM_032501.4(ACSS1):c.632C>T (p.Ala211Val)not specified [RCV004902712]uncertain significance202502364125023641Humanname
597792701CV3647305single nucleotide variantNM_032501.4(ACSS1):c.989T>C (p.Ile330Thr)not specified [RCV004902721]uncertain significance202502150825021508Humanname
598173941CV3938941single nucleotide variantNM_032501.4(ACSS1):c.467C>T (p.Thr156Met)not specified [RCV005309633]uncertain significance202503092325030923Humanname
8637231CV92457single nucleotide variantNM_032501.3(ACSS1):c.670C>T (p.Arg224Trp)Malignant melanoma [RCV000072555]not provided202502360325023603Humanname
150483831CV1247016single nucleotide variantNM_032501.4(ACSS1):c.1435G>A (p.Val479Ile)not provided [RCV001673512]benign202501397825013978Humanname
156084324CV2205580single nucleotide variantNM_032501.4(ACSS1):c.1985C>T (p.Thr662Ile)not specified [RCV004082503]uncertain significance202500784725007847Humanname
155923948CV2217760single nucleotide variantNM_032501.4(ACSS1):c.2014G>A (p.Ala672Thr)not specified [RCV004083940]likely benign202500781825007818Humanname
156080476CV2258264single nucleotide variantNM_032501.4(ACSS1):c.1675C>T (p.Arg559Trp)not specified [RCV004121633]uncertain significance202501284425012844Humanname
155996178CV2277377single nucleotide variantNM_032501.4(ACSS1):c.1547G>T (p.Arg516Leu)not specified [RCV004144797]uncertain significance202501356825013568Humanname
155922659CV2347355single nucleotide variantNM_032501.4(ACSS1):c.2002C>T (p.Pro668Ser)not specified [RCV004207197]uncertain significance202500783025007830Humanname
155926176CV2365707single nucleotide variantNM_032501.4(ACSS1):c.1790T>G (p.Val597Gly)not specified [RCV004214254]uncertain significance202500937025009370Humanname
329359031CV2425476single nucleotide variantNM_032501.4(ACSS1):c.1477G>A (p.Val493Ile)not specified [RCV004251129]uncertain significance202501363825013638Humanname
329384669CV2458333single nucleotide variantNM_032501.4(ACSS1):c.1046G>C (p.Gly349Ala)not specified [RCV004265975]uncertain significance202502145125021451Humanname
401754021CV2716971single nucleotide variantNM_032501.4(ACSS1):c.1213T>C (p.Tyr405His)not specified [RCV004330044]uncertain significance202502004325020043Humanname
401858112CV2774200single nucleotide variantNM_032501.4(ACSS1):c.1805C>T (p.Ala602Val)not specified [RCV004345787]uncertain significance202500935525009355Humanname
401879075CV2778138single nucleotide variantNM_032501.4(ACSS1):c.2006G>C (p.Ser669Thr)not specified [RCV004348077]uncertain significance202500782625007826Humanname
405773531CV3296142single nucleotide variantNM_032501.4(ACSS1):c.1175G>A (p.Arg392Gln)not specified [RCV004435707]uncertain significance202502008125020081Humanname
405773588CV3296152single nucleotide variantNM_032501.4(ACSS1):c.1360G>A (p.Ala454Thr)not specified [RCV004435717]uncertain significance202501405325014053Humanname
405773653CV3296162single nucleotide variantNM_032501.4(ACSS1):c.1556A>G (p.Asp519Gly)not specified [RCV004435727]uncertain significance202501355925013559Humanname
405773670CV3296165single nucleotide variantNM_032501.4(ACSS1):c.1595G>A (p.Gly532Glu)not specified [RCV004435730]uncertain significance202501292425012924Humanname
405773702CV3296170single nucleotide variantNM_032501.4(ACSS1):c.1770A>T (p.Glu590Asp)not specified [RCV004435735]uncertain significance202501260225012602Humanname
405773760CV3296179single nucleotide variantNM_032501.4(ACSS1):c.1838A>G (p.Lys613Arg)not specified [RCV004435744]likely benign202500932225009322Humanname
405773771CV3296181single nucleotide variantNM_032501.4(ACSS1):c.1961G>T (p.Ser654Ile)not specified [RCV004435746]uncertain significance202500787125007871Humanname
407501221CV3421689single nucleotide variantNM_032501.4(ACSS1):c.1738G>A (p.Val580Ile)not specified [RCV004607330]uncertain significance202501263425012634Humanname
407501238CV3421714single nucleotide variantNM_032501.4(ACSS1):c.2047G>A (p.Asp683Asn)not specified [RCV004607334]uncertain significance202500778525007785Humanname
407501243CV3421725single nucleotide variantNM_032501.4(ACSS1):c.1222T>A (p.Ser408Thr)not specified [RCV004607335]uncertain significance202502003425020034Humanname
407475769CV3424803single nucleotide variantNM_032501.4(ACSS1):c.1051C>T (p.Leu351Phe)not specified [RCV004600934]uncertain significance202502144625021446Humanname
597792614CV3647278single nucleotide variantNM_032501.4(ACSS1):c.1438C>A (p.Leu480Ile)not specified [RCV004902698]uncertain significance202501397525013975Humanname
597792849CV3647281single nucleotide variantNM_032501.4(ACSS1):c.1982A>G (p.Asp661Gly)not specified [RCV004902701]uncertain significance202500785025007850Humanname
597792639CV3647316single nucleotide variantNM_032501.4(ACSS1):c.1414C>G (p.Pro472Ala)not specified [RCV004902731]uncertain significance202501399925013999Humanname
598210826CV3938961single nucleotide variantNM_032501.4(ACSS1):c.1967C>T (p.Ala656Val)not specified [RCV005315919]uncertain significance202500786525007865Humanname
598174104CV3938969single nucleotide variantNM_032501.4(ACSS1):c.2027G>C (p.Ser676Thr)not specified [RCV005309657]uncertain significance202500780525007805Humanname
8628476CV83620single nucleotide variantNM_032501.3(ACSS1):c.1244C>T (p.Ser415Leu)Malignant melanoma [RCV000063701]not provided202502001225020012Humanname
8637230CV92456single nucleotide variantNM_032501.3(ACSS1):c.1100C>T (p.Pro367Leu)Malignant melanoma [RCV000072554]not provided202502139725021397Humanname
8586399CV121001single nucleotide variantNM_001252675.1(ACSS1):c.431G>A (p.Arg144Lys)Lung cancer [RCV000101521]uncertain significance202504808525048085Humanname