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33 records found for search term Gnat3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156186383CV2295016single nucleotide variantNM_001102386.3(GNAT3):c.27C>G (p.Ser9Arg)not specified [RCV004156148]uncertain significance78051190080511900Humanname
401755272CV2682433single nucleotide variantNM_001102386.3(GNAT3):c.44G>T (p.Arg15Ile)not specified [RCV004290460]uncertain significance78051188380511883Humanname
156341225CV2268234single nucleotide variantNM_001102386.3(GNAT3):c.248C>T (p.Ala83Val)not specified [RCV004138538]uncertain significance78048859080488590Humanname
155982553CV2371117single nucleotide variantNM_001102386.3(GNAT3):c.221A>C (p.Tyr74Ser)not specified [RCV004220868]uncertain significance78048861780488617Humanname
329369229CV2424765single nucleotide variantNM_001102386.3(GNAT3):c.140G>C (p.Ser47Thr)not specified [RCV004248657]uncertain significance78049462680494626Humanname
405768178CV3262064single nucleotide variantNM_001102386.3(GNAT3):c.113T>A (p.Leu38Gln)not specified [RCV004395453]uncertain significance78051181480511814Humanname
405768183CV3262065single nucleotide variantNM_001102386.3(GNAT3):c.191A>C (p.Gln64Pro)not specified [RCV004395454]uncertain significance78048864780488647Humanname
407519998CV3443572single nucleotide variantNM_001102386.3(GNAT3):c.248C>G (p.Ala83Gly)not specified [RCV004629884]uncertain significance78048859080488590Humanname
598221792CV3893783single nucleotide variantNM_001102386.3(GNAT3):c.1014A>G (p.Ala338=)not provided [RCV005257026]benign78045872280458722Humanname
598264121CV3974359single nucleotide variantNM_001102386.3(GNAT3):c.100G>A (p.Val34Ile)not specified [RCV005348775]uncertain significance78051182780511827Humanname
156319688CV2260874single nucleotide variantNM_001102386.3(GNAT3):c.994G>A (p.Val332Ile)not specified [RCV004125773]uncertain significance78045874280458742Humanname
156165351CV2319857single nucleotide variantNM_001102386.3(GNAT3):c.712G>A (p.Glu238Lys)not specified [RCV004167741]uncertain significance78046251080462510Humanname
156138936CV2354695single nucleotide variantNM_001102386.3(GNAT3):c.696G>T (p.Met232Ile)not specified [RCV004202649]uncertain significance78046252680462526Humanname
155910514CV2366465single nucleotide variantNM_001102386.3(GNAT3):c.898G>A (p.Gly300Arg)not specified [RCV004208444]uncertain significance78045883880458838Humanname
156151320CV2377547single nucleotide variantNM_001102386.3(GNAT3):c.397G>A (p.Asp133Asn)not specified [RCV004225698]uncertain significance78047890580478905Humanname
155997472CV2398720single nucleotide variantNM_001102386.3(GNAT3):c.582G>T (p.Leu194Phe)not specified [RCV004240060]uncertain significance78047425980474259Humanname
401737956CV2700853single nucleotide variantNM_001102386.3(GNAT3):c.776T>C (p.Phe259Ser)not specified [RCV004307128]uncertain significance78046225780462257Humanname
401891796CV2779444single nucleotide variantNM_001102386.3(GNAT3):c.929T>G (p.Leu310Arg)not specified [RCV004351082]uncertain significance78045880780458807Humanname
401896545CV2780923single nucleotide variantNM_001102386.3(GNAT3):c.509A>G (p.Asn170Ser)not specified [RCV004354464]uncertain significance78047433280474332Humanname
405768187CV3262066single nucleotide variantNM_001102386.3(GNAT3):c.299G>T (p.Ser100Ile)not specified [RCV004395455]uncertain significance78048853980488539Humanname
405768192CV3262067single nucleotide variantNM_001102386.3(GNAT3):c.508A>G (p.Asn170Asp)not specified [RCV004395456]uncertain significance78047433380474333Humanname
405768199CV3262068single nucleotide variantNM_001102386.3(GNAT3):c.785C>T (p.Thr262Ile)not specified [RCV004395457]uncertain significance78046224880462248Humanname
405768205CV3262069single nucleotide variantNM_001102386.3(GNAT3):c.828A>C (p.Glu276Asp)not specified [RCV004395458]uncertain significance78046220580462205Humanname
405768211CV3262070single nucleotide variantNM_001102386.3(GNAT3):c.926A>G (p.Asp309Gly)not specified [RCV004395459]uncertain significance78045881080458810Humanname
597788452CV3678209single nucleotide variantNM_001102386.3(GNAT3):c.763A>G (p.Asn255Asp)not specified [RCV004932736]uncertain significance78046227080462270Humanname
597730332CV3678210single nucleotide variantNM_001102386.3(GNAT3):c.594G>A (p.Met198Ile)not specified [RCV004919812]uncertain significance78046262880462628Humanname
597730343CV3678211single nucleotide variantNM_001102386.3(GNAT3):c.575A>G (p.Lys192Arg)not specified [RCV004919813]uncertain significance78047426680474266Humanname
597788420CV3678212single nucleotide variantNM_001102386.3(GNAT3):c.695T>C (p.Met232Thr)not specified [RCV004932737]uncertain significance78046252780462527Humanname
597730355CV3678214single nucleotide variantNM_001102386.3(GNAT3):c.800T>A (p.Phe267Tyr)not specified [RCV004919814]uncertain significance78046223380462233Humanname
598232718CV3974360single nucleotide variantNM_001102386.3(GNAT3):c.362C>T (p.Pro121Leu)not specified [RCV005342643]uncertain significance78047894080478940Humanname
598264124CV3974361single nucleotide variantNM_001102386.3(GNAT3):c.467T>A (p.Leu156His)not specified [RCV005348776]uncertain significance78047437480474374Humanname
405768167CV3262062single nucleotide variantNM_001102386.3(GNAT3):c.1038G>C (p.Glu346Asp)not specified [RCV004395451]uncertain significance78045869880458698Humanname
405768172CV3262063single nucleotide variantNM_001102386.3(GNAT3):c.1060T>G (p.Phe354Val)not specified [RCV004395452]uncertain significance78045867680458676Humanname