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31 records found for search term Slc5a3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598259310CV3911467single nucleotide variantNM_006933.7(SLC5A3):c.68T>C (p.Ile23Thr)not specified [RCV005279555]uncertain significance213409526634095266Humanname
156238417CV2268885single nucleotide variantNM_006933.7(SLC5A3):c.106G>A (p.Val36Met)not specified [RCV004128300]uncertain significance213409530434095304Humanname
156061043CV2323146single nucleotide variantNM_006933.7(SLC5A3):c.274C>T (p.Leu92Phe)not specified [RCV004187550]uncertain significance213409547234095472Humanname
405729059CV3325781single nucleotide variantNM_006933.7(SLC5A3):c.223A>G (p.Ser75Gly)not specified [RCV004464094]uncertain significance213409542134095421Humanname
598259319CV3911469single nucleotide variantNM_006933.7(SLC5A3):c.110G>T (p.Ser37Ile)not specified [RCV005279557]uncertain significance213409530834095308Humanname
15196464CV773306single nucleotide variantNM_006933.7(SLC5A3):c.1203C>T (p.Ser401=)not provided [RCV000934226]likely benign213409640134096401Humanname
156075667CV2291433single nucleotide variantNM_006933.7(SLC5A3):c.554A>G (p.Asp185Gly)not specified [RCV004155762]uncertain significance213409575234095752Humanname
597776148CV3596990single nucleotide variantNM_006933.7(SLC5A3):c.589C>G (p.Leu197Val)not specified [RCV004872722]uncertain significance213409578734095787Humanname
597776152CV3596991single nucleotide variantNM_006933.7(SLC5A3):c.703A>G (p.Asn235Asp)not specified [RCV004872723]uncertain significance213409590134095901Humanname
598259301CV3911465single nucleotide variantNM_006933.7(SLC5A3):c.683T>C (p.Leu228Ser)not specified [RCV005279553]uncertain significance213409588134095881Humanname
156261827CV2204934single nucleotide variantNM_006933.7(SLC5A3):c.1282A>G (p.Ile428Val)not specified [RCV004075174]uncertain significance213409648034096480Humanname
156380365CV2208135single nucleotide variantNM_006933.7(SLC5A3):c.1792C>T (p.Leu598Phe)not specified [RCV004086815]uncertain significance213409699034096990Humanname
156172515CV2337604single nucleotide variantNM_006933.7(SLC5A3):c.1249T>G (p.Phe417Val)not specified [RCV004181168]uncertain significance213409644734096447Humanname
155922497CV2350846single nucleotide variantNM_006933.7(SLC5A3):c.2005C>A (p.Leu669Ile)not specified [RCV004207172]uncertain significance213409720334097203Humanname
401757089CV2678225single nucleotide variantNM_006933.7(SLC5A3):c.1928A>C (p.Glu643Ala)not specified [RCV004296726]uncertain significance213409712634097126Humanname
401772431CV2719640single nucleotide variantNM_006933.7(SLC5A3):c.1195C>T (p.Arg399Cys)not specified [RCV004327303]uncertain significance213409639334096393Humanname
405729021CV3325777single nucleotide variantNM_006933.7(SLC5A3):c.1187A>C (p.Lys396Thr)not specified [RCV004464090]uncertain significance213409638534096385Humanname
405729033CV3325778single nucleotide variantNM_006933.7(SLC5A3):c.1636T>C (p.Phe546Leu)not specified [RCV004464091]uncertain significance213409683434096834Humanname
405729041CV3325779single nucleotide variantNM_006933.7(SLC5A3):c.1804G>T (p.Asp602Tyr)not specified [RCV004464092]uncertain significance213409700234097002Humanname
405729050CV3325780single nucleotide variantNM_006933.7(SLC5A3):c.2055A>C (p.Leu685Phe)not specified [RCV004464093]uncertain significance213409725334097253Humanname
407487409CV3480946single nucleotide variantNM_006933.7(SLC5A3):c.2033T>A (p.Met678Lys)not specified [RCV004674911]uncertain significance213409723134097231Humanname
407488749CV3480947single nucleotide variantNM_006933.7(SLC5A3):c.2059A>T (p.Met687Leu)not specified [RCV004683812]uncertain significance213409725734097257Humanname
597776156CV3596992single nucleotide variantNM_006933.7(SLC5A3):c.1895C>G (p.Ser632Cys)not specified [RCV004872724]uncertain significance213409709334097093Humanname
597724271CV3596993single nucleotide variantNM_006933.7(SLC5A3):c.1261A>G (p.Ile421Val)not specified [RCV004862312]uncertain significance213409645934096459Humanname
597776160CV3596994single nucleotide variantNM_006933.7(SLC5A3):c.1520A>G (p.Lys507Arg)not specified [RCV004872725]uncertain significance213409671834096718Humanname
597776164CV3596995single nucleotide variantNM_006933.7(SLC5A3):c.1723T>C (p.Cys575Arg)not specified [RCV004872726]uncertain significance213409692134096921Humanname
598259287CV3911461single nucleotide variantNM_006933.7(SLC5A3):c.1516A>G (p.Ile506Val)not specified [RCV005279550]uncertain significance213409671434096714Humanname
598237515CV3911462single nucleotide variantNM_006933.7(SLC5A3):c.1204G>A (p.Ala402Thr)not specified [RCV005275669]uncertain significance213409640234096402Humanname
598259292CV3911463single nucleotide variantNM_006933.7(SLC5A3):c.1082T>C (p.Val361Ala)not specified [RCV005279551]uncertain significance213409628034096280Humanname
598259297CV3911464single nucleotide variantNM_006933.7(SLC5A3):c.1133A>G (p.Asp378Gly)not specified [RCV005279552]uncertain significance213409633134096331Humanname
598259314CV3911468single nucleotide variantNM_006933.7(SLC5A3):c.2003G>A (p.Ser668Asn)not specified [RCV005279556]uncertain significance213409720134097201Humanname