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Variants search result for Homo sapiens
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72 records found for search term Slc16a3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401771801CV2722951single nucleotide variantNM_004207.4(SLC16A3):c.8G>T (p.Gly3Val)not specified [RCV004327130]uncertain significance178223601682236016Humanname
401907946CV2818126single nucleotide variantNM_004207.4(SLC16A3):c.297G>A (p.Ser99=)not provided [RCV003422993]likely benign178223680282236802Humanname
598268494CV3921633single nucleotide variantNM_004207.4(SLC16A3):c.13G>A (p.Val5Met)not specified [RCV005281778]uncertain significance178223602182236021Humanname
15195362CV727593single nucleotide variantNM_004207.4(SLC16A3):c.267C>T (p.Pro89=)not provided [RCV000889483]likely benign178223677282236772Humanname
156138125CV2202798single nucleotide variantNM_004207.4(SLC16A3):c.37G>A (p.Val13Ile)not specified [RCV004073660]likely benign178223604582236045Humanname
156165928CV2319902single nucleotide variantNM_004207.4(SLC16A3):c.70G>A (p.Val24Met)not specified [RCV004167782]uncertain significance178223607882236078Humanname
598199957CV3921631single nucleotide variantNM_004207.4(SLC16A3):c.79G>A (p.Gly27Ser)not specified [RCV005268470]uncertain significance178223608782236087Humanname
15194325CV704510single nucleotide variantNM_004207.4(SLC16A3):c.831G>A (p.Ala277=)not provided [RCV000955615]benign178223760182237601Humanname
15145329CV741242single nucleotide variantNM_004207.4(SLC16A3):c.44C>T (p.Ala15Val)not provided [RCV000900144]benign178223605282236052Humanname
156186439CV2292391single nucleotide variantNM_004207.4(SLC16A3):c.191C>T (p.Ser64Phe)not specified [RCV004150195]uncertain significance178223619982236199Humanname
401771819CV2693532single nucleotide variantNM_004207.4(SLC16A3):c.186G>C (p.Trp62Cys)not specified [RCV004297516]uncertain significance178223619482236194Humanname
401907947CV2818127single nucleotide variantNM_004207.4(SLC16A3):c.1275G>A (p.Glu425=)not provided [RCV003422994]likely benign178223885382238853Humanname
401907950CV2818128single nucleotide variantNM_004207.4(SLC16A3):c.1362C>T (p.Asn454=)not provided [RCV003422995]likely benign178223894082238940Humanname
405711060CV3328878single nucleotide variantNM_004207.4(SLC16A3):c.251G>A (p.Arg84His)not specified [RCV004448482]uncertain significance178223675682236756Humanname
407519500CV3477212single nucleotide variantNM_004207.4(SLC16A3):c.166G>C (p.Gly56Arg)not specified [RCV004676536]uncertain significance178223617482236174Humanname
598268515CV3921637single nucleotide variantNM_004207.4(SLC16A3):c.233G>A (p.Cys78Tyr)not specified [RCV005281782]uncertain significance178223673882236738Humanname
155958943CV2197582single nucleotide variantNM_004207.4(SLC16A3):c.817A>G (p.Ile273Val)not specified [RCV004081300]uncertain significance178223758782237587Humanname
156172427CV2267895single nucleotide variantNM_004207.4(SLC16A3):c.571T>G (p.Cys191Gly)not specified [RCV004136188]uncertain significance178223734182237341Humanname
156339173CV2271379single nucleotide variantNM_004207.4(SLC16A3):c.875C>T (p.Pro292Leu)not specified [RCV004136491]uncertain significance178223764582237645Humanname
155945150CV2291988single nucleotide variantNM_004207.4(SLC16A3):c.608C>T (p.Thr203Met)not specified [RCV004158492]uncertain significance178223737882237378Humanname
156053516CV2320387single nucleotide variantNM_004207.4(SLC16A3):c.703G>A (p.Ala235Thr)not specified [RCV004178546]uncertain significance178223747382237473Humanname
155916141CV2336092single nucleotide variantNM_004207.4(SLC16A3):c.928C>G (p.Leu310Val)not specified [RCV004189688]uncertain significance178223769882237698Humanname
155912842CV2341657single nucleotide variantNM_004207.4(SLC16A3):c.326G>A (p.Arg109Gln)not specified [RCV004182581]uncertain significance178223683182236831Humanname
156342201CV2345102single nucleotide variantNM_004207.4(SLC16A3):c.494C>T (p.Pro165Leu)not specified [RCV004193375]uncertain significance178223726482237264Humanname
156146333CV2357929single nucleotide variantNM_004207.4(SLC16A3):c.646C>T (p.Arg216Cys)not specified [RCV004209713]uncertain significance178223741682237416Humanname
155917073CV2366822single nucleotide variantNM_004207.4(SLC16A3):c.734C>T (p.Pro245Leu)not specified [RCV004210810]uncertain significance178223750482237504Humanname
156043138CV2381520single nucleotide variantNM_004207.4(SLC16A3):c.626G>A (p.Gly209Glu)not specified [RCV004229998]uncertain significance178223739682237396Humanname
156115212CV2392270single nucleotide variantNM_004207.4(SLC16A3):c.590T>C (p.Met197Thr)not specified [RCV004243876]uncertain significance178223736082237360Humanname
329392401CV2438919single nucleotide variantNM_004207.4(SLC16A3):c.632C>G (p.Pro211Arg)not specified [RCV004264441]uncertain significance178223740282237402Humanname
329363148CV2464678single nucleotide variantNM_004207.4(SLC16A3):c.818T>C (p.Ile273Thr)not specified [RCV004282868]uncertain significance178223758882237588Humanname
401731719CV2693956single nucleotide variantNM_004207.4(SLC16A3):c.836C>T (p.Pro279Leu)not specified [RCV004300250]uncertain significance178223760682237606Humanname
401730000CV2700356single nucleotide variantNM_004207.4(SLC16A3):c.949G>A (p.Asp317Asn)not specified [RCV004311012]uncertain significance178223771982237719Humanname
401739906CV2709725single nucleotide variantNM_004207.4(SLC16A3):c.872G>A (p.Arg291Gln)not specified [RCV004320718]uncertain significance178223764282237642Humanname
401772117CV2719538single nucleotide variantNM_004207.4(SLC16A3):c.647G>A (p.Arg216His)not specified [RCV004327222]uncertain significance178223741782237417Humanname
401896990CV2785476single nucleotide variantNM_004207.4(SLC16A3):c.520T>G (p.Tyr174Asp)not specified [RCV004363006]uncertain significance178223729082237290Humanname
401898362CV2787730single nucleotide variantNM_004207.4(SLC16A3):c.652C>A (p.Leu218Ile)not specified [RCV004356645]uncertain significance178223742282237422Humanname
405711070CV3328879single nucleotide variantNM_004207.4(SLC16A3):c.365C>T (p.Thr122Met)not specified [RCV004448483]uncertain significance178223687082236870Humanname
405711077CV3328880single nucleotide variantNM_004207.4(SLC16A3):c.535G>A (p.Gly179Ser)not specified [RCV004448484]uncertain significance178223730582237305Humanname
405711081CV3328881single nucleotide variantNM_004207.4(SLC16A3):c.829G>A (p.Ala277Thr)not specified [RCV004448485]uncertain significance178223759982237599Humanname
405711088CV3328882single nucleotide variantNM_004207.4(SLC16A3):c.900C>G (p.Phe300Leu)not specified [RCV004448486]uncertain significance178223767082237670Humanname
405711095CV3328883single nucleotide variantNM_004207.4(SLC16A3):c.914A>G (p.Asn305Ser)not specified [RCV004448487]uncertain significance178223768482237684Humanname
407503102CV3477211single nucleotide variantNM_004207.4(SLC16A3):c.647G>T (p.Arg216Leu)not specified [RCV004670146]uncertain significance178223741782237417Humanname
407503106CV3477213single nucleotide variantNM_004207.4(SLC16A3):c.403A>G (p.Ile135Val)not specified [RCV004670147]uncertain significance178223717382237173Humanname
407503110CV3477214single nucleotide variantNM_004207.4(SLC16A3):c.638C>A (p.Pro213His)not specified [RCV004670148]uncertain significance178223740882237408Humanname
407503113CV3477215single nucleotide variantNM_004207.4(SLC16A3):c.414C>G (p.Asn138Lys)not specified [RCV004670149]uncertain significance178223718482237184Humanname
407503117CV3477216single nucleotide variantNM_004207.4(SLC16A3):c.629C>T (p.Pro210Leu)not specified [RCV004670150]likely benign178223739982237399Humanname
597675497CV3599647single nucleotide variantNM_004207.4(SLC16A3):c.614A>G (p.Gln205Arg)not specified [RCV004856866]likely benign178223738482237384Humanname
597675506CV3599648single nucleotide variantNM_004207.4(SLC16A3):c.517C>T (p.Arg173Cys)not specified [RCV004856867]uncertain significance178223728782237287Humanname
597675517CV3599649single nucleotide variantNM_004207.4(SLC16A3):c.523G>A (p.Gly175Ser)not specified [RCV004856868]uncertain significance178223729382237293Humanname
598268500CV3921634single nucleotide variantNM_004207.4(SLC16A3):c.922G>A (p.Ala308Thr)not specified [RCV005281779]likely benign178223769282237692Humanname
598268505CV3921635single nucleotide variantNM_004207.4(SLC16A3):c.739G>A (p.Val247Met)not specified [RCV005281780]uncertain significance178223750982237509Humanname
598268510CV3921636single nucleotide variantNM_004207.4(SLC16A3):c.772G>T (p.Val258Leu)not specified [RCV005281781]uncertain significance178223754282237542Humanname
598199969CV3921639single nucleotide variantNM_004207.4(SLC16A3):c.937T>C (p.Ser313Pro)not specified [RCV005268472]uncertain significance178223770782237707Humanname
156191783CV2206204single nucleotide variantNM_004207.4(SLC16A3):c.1105G>A (p.Val369Ile)not specified [RCV004080642]likely benign178223787582237875Humanname
155925052CV2248934single nucleotide variantNM_004207.4(SLC16A3):c.1187T>G (p.Leu396Arg)not specified [RCV004115935]uncertain significance178223876582238765Humanname
155970255CV2262209single nucleotide variantNM_004207.4(SLC16A3):c.1154T>C (p.Met385Thr)not specified [RCV004126637]uncertain significance178223873282238732Humanname
156069389CV2292748single nucleotide variantNM_004207.4(SLC16A3):c.1381C>G (p.Pro461Ala)not specified [RCV004154414]uncertain significance178223895982238959Humanname
155922402CV2350827single nucleotide variantNM_004207.4(SLC16A3):c.1270G>A (p.Ala424Thr)not specified [RCV004207155]uncertain significance178223884882238848Humanname
155989622CV2352243single nucleotide variantNM_004207.4(SLC16A3):c.1108G>A (p.Gly370Arg)not specified [RCV004200719]uncertain significance178223787882237878Humanname
156258756CV2383845single nucleotide variantNM_004207.4(SLC16A3):c.1305C>A (p.Asp435Glu)not specified [RCV004231708]uncertain significance178223888382238883Humanname
156189449CV2395686single nucleotide variantNM_004207.4(SLC16A3):c.1172C>T (p.Ala391Val)not specified [RCV004234871]uncertain significance178223875082238750Humanname
401869797CV2792183single nucleotide variantNM_004207.4(SLC16A3):c.1232G>A (p.Arg411Lys)not specified [RCV004361392]uncertain significance178223881082238810Humanname
401870792CV2792417single nucleotide variantNM_004207.4(SLC16A3):c.1322G>C (p.Arg441Pro)not specified [RCV004363170]uncertain significance178223890082238900Humanname
405711034CV3328874single nucleotide variantNM_004207.4(SLC16A3):c.1118C>T (p.Ser373Leu)not specified [RCV004448478]uncertain significance178223788882237888Humanname
405711041CV3328875single nucleotide variantNM_004207.4(SLC16A3):c.1312G>A (p.Val438Met)not specified [RCV004448479]uncertain significance178223889082238890Humanname
405711048CV3328876single nucleotide variantNM_004207.4(SLC16A3):c.1315G>C (p.Asp439His)not specified [RCV004448480]uncertain significance178223889382238893Humanname
405711053CV3328877single nucleotide variantNM_004207.4(SLC16A3):c.1364G>A (p.Gly455Glu)not specified [RCV004448481]uncertain significance178223894282238942Humanname
597675529CV3599650single nucleotide variantNM_004207.4(SLC16A3):c.1309G>C (p.Gly437Arg)not specified [RCV004856869]likely benign178223888782238887Humanname
597675549CV3599652single nucleotide variantNM_004207.4(SLC16A3):c.1192T>A (p.Ser398Thr)not specified [RCV004856871]uncertain significance178223877082238770Humanname
597675559CV3599653single nucleotide variantNM_004207.4(SLC16A3):c.1159G>A (p.Val387Met)not specified [RCV004856872]uncertain significance178223873782238737Humanname
598199963CV3921632single nucleotide variantNM_004207.4(SLC16A3):c.1273G>A (p.Glu425Lys)not specified [RCV005268471]uncertain significance178223885182238851Humanname
598268522CV3921638single nucleotide variantNM_004207.4(SLC16A3):c.1382C>T (p.Pro461Leu)not specified [RCV005281783]uncertain significance178223896082238960Humanname