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62 records found for search term Trim35
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401758374CV2694071single nucleotide variantNM_171982.5(TRIM35):c.8G>A (p.Arg3Gln)not specified [RCV004302506]uncertain significance82731122827311228Humanname
155932502CV2364405single nucleotide variantNM_171982.5(TRIM35):c.17A>G (p.Asp6Gly)not specified [RCV004223616]uncertain significance82731121927311219Humanname
407453756CV3490497single nucleotide variantNM_171982.5(TRIM35):c.26C>T (p.Pro9Leu)not specified [RCV004684655]uncertain significance82731121027311210Humanname
597801752CV3617709single nucleotide variantNM_171982.5(TRIM35):c.19G>A (p.Val7Met)not specified [RCV004880884]uncertain significance82731121727311217Humanname
15185974CV700545single nucleotide variantNM_171982.5(TRIM35):c.363C>T (p.Cys121=)not provided [RCV000953142]benign82731087327310873Humanname
15145934CV711473single nucleotide variantNM_171982.5(TRIM35):c.630C>T (p.Ala210=)not provided [RCV000967082]benign82729421227294212Humanname
155983247CV2273058single nucleotide variantNM_171982.5(TRIM35):c.188G>A (p.Arg63His)not specified [RCV004137708]uncertain significance82731104827311048Humanname
329376822CV2428557single nucleotide variantNM_171982.5(TRIM35):c.157G>T (p.Val53Leu)not specified [RCV004253341]uncertain significance82731107927311079Humanname
405790248CV3336929single nucleotide variantNM_171982.5(TRIM35):c.259G>A (p.Ala87Thr)not specified [RCV004473808]uncertain significance82731097727310977Humanname
597801756CV3617711single nucleotide variantNM_171982.5(TRIM35):c.161C>T (p.Ser54Leu)not specified [RCV004880886]uncertain significance82731107527311075Humanname
598274126CV3935428single nucleotide variantNM_171982.5(TRIM35):c.248T>G (p.Leu83Arg)not specified [RCV005303772]uncertain significance82731098827310988Humanname
156067391CV2236970single nucleotide variantNM_171982.5(TRIM35):c.563G>A (p.Arg188Gln)not specified [RCV004112964]uncertain significance82729427927294279Humanname
156060367CV2239434single nucleotide variantNM_171982.5(TRIM35):c.664G>A (p.Glu222Lys)not specified [RCV004114156]uncertain significance82729417827294178Humanname
155971428CV2262337single nucleotide variantNM_171982.5(TRIM35):c.747C>A (p.Asp249Glu)not specified [RCV004128528]uncertain significance82729409527294095Humanname
155902912CV2274790single nucleotide variantNM_171982.5(TRIM35):c.771G>T (p.Lys257Asn)not specified [RCV004139134]uncertain significance82729017027290170Humanname
156277717CV2286617single nucleotide variantNM_171982.5(TRIM35):c.500G>A (p.Arg167His)not specified [RCV004142467]uncertain significance82729849527298495Humanname
156059652CV2316999single nucleotide variantNM_171982.5(TRIM35):c.443G>T (p.Cys148Phe)not specified [RCV004174496]uncertain significance82729855227298552Humanname
156009077CV2361953single nucleotide variantNM_171982.5(TRIM35):c.305G>A (p.Arg102His)not specified [RCV004207721]uncertain significance82731093127310931Humanname
155958544CV2395206single nucleotide variantNM_171982.5(TRIM35):c.584G>A (p.Arg195His)not specified [RCV004236874]uncertain significance82729425827294258Humanname
329371351CV2431901single nucleotide variantNM_171982.5(TRIM35):c.421G>A (p.Ala141Thr)not specified [RCV004255034]uncertain significance82731081527310815Humanname
329390586CV2455322single nucleotide variantNM_171982.5(TRIM35):c.626T>C (p.Met209Thr)not specified [RCV004274830]uncertain significance82729421627294216Humanname
329395522CV2458436single nucleotide variantNM_171982.5(TRIM35):c.965C>G (p.Thr322Ser)not specified [RCV004266064]uncertain significance82728806727288067Humanname
329374094CV2463308single nucleotide variantNM_171982.5(TRIM35):c.467G>A (p.Arg156Gln)not specified [RCV004275368]uncertain significance82729852827298528Humanname
401873063CV2793193single nucleotide variantNM_171982.5(TRIM35):c.927C>A (p.Asn309Lys)not specified [RCV004360498]uncertain significance82728810527288105Humanname
405790253CV3336931single nucleotide variantNM_171982.5(TRIM35):c.433C>T (p.Arg145Trp)not specified [RCV004473810]uncertain significance82731080327310803Humanname
405790256CV3336932single nucleotide variantNM_171982.5(TRIM35):c.445A>G (p.Arg149Gly)not specified [RCV004473811]uncertain significance82729855027298550Humanname
405790259CV3336933single nucleotide variantNM_171982.5(TRIM35):c.643C>G (p.Gln215Glu)not specified [RCV004473812]uncertain significance82729419927294199Humanname
597801745CV3617705single nucleotide variantNM_171982.5(TRIM35):c.569A>G (p.Glu190Gly)not specified [RCV004880880]uncertain significance82729427327294273Humanname
598202603CV3935425single nucleotide variantNM_171982.5(TRIM35):c.979C>T (p.His327Tyr)not specified [RCV005290403]uncertain significance82728805327288053Humanname
598274124CV3935426single nucleotide variantNM_171982.5(TRIM35):c.334T>C (p.Cys112Arg)not specified [RCV005303771]uncertain significance82731090227310902Humanname
598202609CV3935427single nucleotide variantNM_171982.5(TRIM35):c.763A>G (p.Lys255Glu)not specified [RCV005290404]uncertain significance82729017827290178Humanname
156138710CV2211961single nucleotide variantNM_171982.5(TRIM35):c.1069G>A (p.Ala357Thr)not specified [RCV004087087]uncertain significance82728796327287963Humanname
156105557CV2257210single nucleotide variantNM_171982.5(TRIM35):c.1202G>A (p.Arg401His)not specified [RCV004123420]uncertain significance82728783027287830Humanname
156168318CV2315378single nucleotide variantNM_171982.5(TRIM35):c.1238C>T (p.Ser413Leu)not specified [RCV004167346]uncertain significance82728779427287794Humanname
155965262CV2330551single nucleotide variantNM_171982.5(TRIM35):c.1354A>G (p.Thr452Ala)not specified [RCV004181114]uncertain significance82728767827287678Humanname
156066959CV2340936single nucleotide variantNM_171982.5(TRIM35):c.1064C>T (p.Ser355Leu)not specified [RCV004181430]uncertain significance82728796827287968Humanname
156125193CV2350170single nucleotide variantNM_171982.5(TRIM35):c.1127G>A (p.Arg376His)not specified [RCV004200085]uncertain significance82728790527287905Humanname
155929788CV2360967single nucleotide variantNM_171982.5(TRIM35):c.1288G>T (p.Val430Leu)not specified [RCV004216166]uncertain significance82728774427287744Humanname
156078488CV2375185single nucleotide variantNM_171982.5(TRIM35):c.1213G>A (p.Val405Met)not specified [RCV004230225]uncertain significance82728781927287819Humanname
156392742CV2386646single nucleotide variantNM_171982.5(TRIM35):c.1435C>T (p.Arg479Cys)not specified [RCV004230987]uncertain significance82728759727287597Humanname
156087290CV2388117single nucleotide variantNM_171982.5(TRIM35):c.1121G>A (p.Arg374His)not specified [RCV004241235]uncertain significance82728791127287911Humanname
155930648CV2399697single nucleotide variantNM_171982.5(TRIM35):c.1142C>T (p.Ala381Val)not specified [RCV004245516]uncertain significance82728789027287890Humanname
329364594CV2443724single nucleotide variantNM_171982.5(TRIM35):c.1205C>T (p.Thr402Met)not specified [RCV004256024]uncertain significance82728782727287827Humanname
401746893CV2698727single nucleotide variantNM_171982.5(TRIM35):c.1243C>T (p.Pro415Ser)not specified [RCV004301183]uncertain significance82728778927287789Humanname
401748881CV2706218single nucleotide variantNM_171982.5(TRIM35):c.1171G>T (p.Asp391Tyr)not specified [RCV004314891]uncertain significance82728786127287861Humanname
401729331CV2732971single nucleotide variantNM_171982.5(TRIM35):c.1205C>G (p.Thr402Arg)not specified [RCV004331147]uncertain significance82728782727287827Humanname
401861969CV2766525single nucleotide variantNM_171982.5(TRIM35):c.1198T>G (p.Cys400Gly)not specified [RCV004347145]uncertain significance82728783427287834Humanname
401884641CV2786532single nucleotide variantNM_171982.5(TRIM35):c.1170C>A (p.His390Gln)not specified [RCV004363685]uncertain significance82728786227287862Humanname
405790233CV3336924single nucleotide variantNM_171982.5(TRIM35):c.1013G>A (p.Arg338His)not specified [RCV004473803]uncertain significance82728801927288019Humanname
405790236CV3336925single nucleotide variantNM_171982.5(TRIM35):c.1279C>T (p.Arg427Cys)not specified [RCV004473804]uncertain significance82728775327287753Humanname
405790239CV3336926single nucleotide variantNM_171982.5(TRIM35):c.1406C>T (p.Ala469Val)not specified [RCV004473805]uncertain significance82728762627287626Humanname
405790242CV3336927single nucleotide variantNM_171982.5(TRIM35):c.1414G>A (p.Ala472Thr)not specified [RCV004473806]uncertain significance82728761827287618Humanname
405790245CV3336928single nucleotide variantNM_171982.5(TRIM35):c.1438A>G (p.Ile480Val)not specified [RCV004473807]uncertain significance82728759427287594Humanname
407453748CV3490495single nucleotide variantNM_171982.5(TRIM35):c.1069G>C (p.Ala357Pro)not specified [RCV004684653]uncertain significance82728796327287963Humanname
407453752CV3490496single nucleotide variantNM_171982.5(TRIM35):c.1405G>A (p.Ala469Thr)not specified [RCV004684654]uncertain significance82728762727287627Humanname
597801747CV3617706single nucleotide variantNM_171982.5(TRIM35):c.1136C>T (p.Ser379Leu)not specified [RCV004880881]uncertain significance82728789627287896Humanname
597801749CV3617707single nucleotide variantNM_171982.5(TRIM35):c.1231G>A (p.Val411Met)not specified [RCV004880882]uncertain significance82728780127287801Humanname
597801750CV3617708single nucleotide variantNM_171982.5(TRIM35):c.1178G>A (p.Arg393His)not specified [RCV004880883]uncertain significance82728785427287854Humanname
597801754CV3617710single nucleotide variantNM_171982.5(TRIM35):c.1091G>A (p.Gly364Glu)not specified [RCV004880885]uncertain significance82728794127287941Humanname
598274120CV3935422single nucleotide variantNM_171982.5(TRIM35):c.1126C>T (p.Arg376Cys)not specified [RCV005303769]uncertain significance82728790627287906Humanname
598274122CV3935423single nucleotide variantNM_171982.5(TRIM35):c.1286G>A (p.Arg429His)not specified [RCV005303770]uncertain significance82728774627287746Humanname
598274129CV3935429single nucleotide variantNM_171982.5(TRIM35):c.1363G>A (p.Ala455Thr)not specified [RCV005303773]uncertain significance82728766927287669Humanname