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Variants search result for Homo sapiens
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54 records found for search term Slc13a2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407519448CV3477141single nucleotide variantNM_003984.4(SLC13A2):c.232-51G>Anot specified [RCV004676513]uncertain significance172849040328490403Humanname
156099179CV2392845single nucleotide variantNM_003984.4(SLC13A2):c.19G>A (p.Ala7Thr)not specified [RCV004247204]uncertain significance172847373128473731Humanname
401755202CV2732661single nucleotide variantNM_003984.4(SLC13A2):c.13T>C (p.Trp5Arg)not specified [RCV004332595]uncertain significance172847372528473725Humanname
155961223CV2311881single nucleotide variantNM_003984.4(SLC13A2):c.91G>A (p.Val31Ile)not specified [RCV004170717]likely benign172847380328473803Humanname
329392838CV2439217single nucleotide variantNM_003984.4(SLC13A2):c.295G>A (p.Ala99Thr)not specified [RCV004266488]uncertain significance172849051728490517Humanname
401896616CV2791765single nucleotide variantNM_003984.4(SLC13A2):c.226T>C (p.Ser76Pro)not specified [RCV004353085]uncertain significance172848933728489337Humanname
407502924CV3477143single nucleotide variantNM_003984.4(SLC13A2):c.250A>G (p.Lys84Glu)not specified [RCV004670100]uncertain significance172849047228490472Humanname
597740615CV3599494single nucleotide variantNM_003984.4(SLC13A2):c.217G>A (p.Val73Met)not specified [RCV004864694]likely benign172848932828489328Humanname
597674003CV3599498single nucleotide variantNM_003984.4(SLC13A2):c.289G>A (p.Ala97Thr)not specified [RCV004856724]uncertain significance172849051128490511Humanname
597674025CV3599500single nucleotide variantNM_003984.4(SLC13A2):c.229G>A (p.Glu77Lys)not specified [RCV004856726]uncertain significance172848934028489340Humanname
8621475CV75449single nucleotide variantNM_003984.4(SLC13A2):c.1326G>A (p.Glu442=)not provided [RCV000054671]uncertain significance172849567228495672Humanname
156026782CV2199178single nucleotide variantNM_003984.4(SLC13A2):c.778G>A (p.Val260Met)not specified [RCV004080567]uncertain significance172849175228491752Humanname
156196431CV2241541single nucleotide variantNM_003984.4(SLC13A2):c.790G>A (p.Ala264Thr)not specified [RCV004104438]uncertain significance172849176428491764Humanname
156154846CV2266104single nucleotide variantNM_003984.4(SLC13A2):c.883C>T (p.Arg295Trp)not specified [RCV004128699]uncertain significance172849357528493575Humanname
156192012CV2301854single nucleotide variantNM_003984.4(SLC13A2):c.359G>A (p.Arg120Gln)not specified [RCV004156647]uncertain significance172849058128490581Humanname
156210346CV2314251single nucleotide variantNM_003984.4(SLC13A2):c.607T>G (p.Ser203Ala)not specified [RCV004166614]uncertain significance172849146928491469Humanname
156300506CV2322495single nucleotide variantNM_003984.4(SLC13A2):c.893T>C (p.Phe298Ser)not specified [RCV004180616]uncertain significance172849358528493585Humanname
155918464CV2333006single nucleotide variantNM_003984.4(SLC13A2):c.904G>C (p.Glu302Gln)not specified [RCV004194306]uncertain significance172849359628493596Humanname
156036947CV2374026single nucleotide variantNM_003984.4(SLC13A2):c.826A>G (p.Ile276Val)not specified [RCV004227152]uncertain significance172849180028491800Humanname
156188491CV2395445single nucleotide variantNM_003984.4(SLC13A2):c.410T>C (p.Met137Thr)not specified [RCV004241316]uncertain significance172849074228490742Humanname
329374018CV2447542single nucleotide variantNM_003984.4(SLC13A2):c.599C>T (p.Thr200Met)not specified [RCV004255899]uncertain significance172849146128491461Humanname
401863791CV2770830single nucleotide variantNM_003984.4(SLC13A2):c.545C>A (p.Pro182Gln)not specified [RCV004349862]uncertain significance172849087728490877Humanname
401882865CV2775136single nucleotide variantNM_003984.4(SLC13A2):c.952G>A (p.Glu318Lys)not specified [RCV004346494]uncertain significance172849364428493644Humanname
401890825CV2778374single nucleotide variantNM_003984.4(SLC13A2):c.959G>A (p.Arg320Lys)not specified [RCV004344060]likely benign172849365128493651Humanname
405767262CV3328730single nucleotide variantNM_003984.4(SLC13A2):c.391G>C (p.Val131Leu)not specified [RCV004456350]uncertain significance172849072328490723Humanname
405767268CV3328731single nucleotide variantNM_003984.4(SLC13A2):c.519C>A (p.Asn173Lys)not specified [RCV004456351]uncertain significance172849085128490851Humanname
407502914CV3477140single nucleotide variantNM_003984.4(SLC13A2):c.485C>T (p.Ser162Leu)not specified [RCV004670098]uncertain significance172849081728490817Humanname
407502939CV3477147single nucleotide variantNM_003984.4(SLC13A2):c.323G>T (p.Arg108Leu)not specified [RCV004670103]uncertain significance172849054528490545Humanname
597740620CV3599495single nucleotide variantNM_003984.4(SLC13A2):c.899T>A (p.Ile300Asn)not specified [RCV004864695]uncertain significance172849359128493591Humanname
597673995CV3599497single nucleotide variantNM_003984.4(SLC13A2):c.692T>G (p.Ile231Ser)not specified [RCV004856723]uncertain significance172849155428491554Humanname
597674014CV3599499single nucleotide variantNM_003984.4(SLC13A2):c.724C>T (p.Pro242Ser)not specified [RCV004856725]uncertain significance172849158628491586Humanname
597674045CV3599502single nucleotide variantNM_003984.4(SLC13A2):c.904G>A (p.Glu302Lys)not specified [RCV004856728]uncertain significance172849359628493596Humanname
598199845CV3921528single nucleotide variantNM_003984.4(SLC13A2):c.700A>T (p.Ile234Phe)not specified [RCV005268455]uncertain significance172849156228491562Humanname
156065102CV2240271single nucleotide variantNM_003984.4(SLC13A2):c.1180G>T (p.Asp394Tyr)not specified [RCV004112833]uncertain significance172849409928494099Humanname
156339159CV2271378single nucleotide variantNM_003984.4(SLC13A2):c.1253C>T (p.Pro418Leu)not specified [RCV004136490]uncertain significance172849445728494457Humanname
156261907CV2319750single nucleotide variantNM_003984.4(SLC13A2):c.1471G>A (p.Ala491Thr)not specified [RCV004187285]uncertain significance172849645028496450Humanname
329380936CV2440485single nucleotide variantNM_003984.4(SLC13A2):c.1613G>A (p.Arg538Gln)not specified [RCV004256411]uncertain significance172849710328497103Humanname
329387074CV2452836single nucleotide variantNM_003984.4(SLC13A2):c.1502T>A (p.Val501Asp)not specified [RCV004275365]uncertain significance172849648128496481Humanname
329352426CV2453006single nucleotide variantNM_003984.4(SLC13A2):c.1697A>T (p.His566Leu)not specified [RCV004277626]uncertain significance172849718728497187Humanname
401877995CV2786927single nucleotide variantNM_003984.4(SLC13A2):c.1553C>T (p.Ala518Val)not specified [RCV004366067]uncertain significance172849653228496532Humanname
405767243CV3328727single nucleotide variantNM_003984.4(SLC13A2):c.1112G>A (p.Gly371Glu)not specified [RCV004456347]uncertain significance172849403128494031Humanname
405767248CV3328728single nucleotide variantNM_003984.4(SLC13A2):c.1540A>C (p.Met514Leu)not specified [RCV004456348]uncertain significance172849651928496519Humanname
405767255CV3328729single nucleotide variantNM_003984.4(SLC13A2):c.1754C>T (p.Ala585Val)not specified [RCV004456349]uncertain significance172849724428497244Humanname
407502919CV3477142single nucleotide variantNM_003984.4(SLC13A2):c.1043C>T (p.Pro348Leu)not specified [RCV004670099]uncertain significance172849373528493735Humanname
407502929CV3477145single nucleotide variantNM_003984.4(SLC13A2):c.1360G>A (p.Val454Met)not specified [RCV004670101]uncertain significance172849570628495706Humanname
407502935CV3477146single nucleotide variantNM_003984.4(SLC13A2):c.1753G>A (p.Ala585Thr)not specified [RCV004670102]uncertain significance172849724328497243Humanname
597740624CV3599496single nucleotide variantNM_003984.4(SLC13A2):c.1559C>T (p.Pro520Leu)not specified [RCV004864696]uncertain significance172849653828496538Humanname
597674036CV3599501single nucleotide variantNM_003984.4(SLC13A2):c.1475A>G (p.Gln492Arg)not specified [RCV004856727]uncertain significance172849645428496454Humanname
597674063CV3599504single nucleotide variantNM_003984.4(SLC13A2):c.1099A>T (p.Met367Leu)not specified [RCV004856730]uncertain significance172849401828494018Humanname
598268022CV3921529single nucleotide variantNM_003984.4(SLC13A2):c.1018G>A (p.Val340Met)not specified [RCV005281690]uncertain significance172849371028493710Humanname
598268028CV3921530single nucleotide variantNM_003984.4(SLC13A2):c.1516A>G (p.Thr506Ala)not specified [RCV005281691]uncertain significance172849649528496495Humanname
598268034CV3921531single nucleotide variantNM_003984.4(SLC13A2):c.1637T>C (p.Ile546Thr)not specified [RCV005281692]uncertain significance172849712728497127Humanname
8621476CV75450single nucleotide variantNM_003984.4(SLC13A2):c.1370C>T (p.Pro457Leu)not provided [RCV000054672]uncertain significance172849571628495716Humanname
8636056CV91279single nucleotide variantNM_001145975.1(SLC13A2):c.400G>A (p.Asp134Asn)Malignant melanoma [RCV000071377]not provided172849047528490475Humanname