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42 records found for search term Fcrl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8574931CV109270single nucleotide variantNM_001159397.1(FCRL1):c.32-4195A>GLung cancer [RCV000089795]uncertain significance1157811317157811317Humanname
598229672CV3959152single nucleotide variantNM_052938.5(FCRL1):c.77C>T (p.Ser26Phe)not specified [RCV005342114]uncertain significance1157804087157804087Humanname
155909035CV2350419single nucleotide variantNM_052938.5(FCRL1):c.248C>T (p.Ser83Leu)not specified [RCV004204796]uncertain significance1157803916157803916Humanname
156089371CV2359365single nucleotide variantNM_052938.5(FCRL1):c.209A>G (p.Lys70Arg)not specified [RCV004212644]uncertain significance1157803955157803955Humanname
405742322CV3256907single nucleotide variantNM_052938.5(FCRL1):c.110C>T (p.Thr37Met)not specified [RCV004391523]uncertain significance1157804054157804054Humanname
405742336CV3256909single nucleotide variantNM_052938.5(FCRL1):c.1224C>T (p.Ser408=)not specified [RCV004391525]likely benign1157796165157796165Humanname
405742341CV3256910single nucleotide variantNM_052938.5(FCRL1):c.171C>A (p.Asp57Glu)not specified [RCV004391526]uncertain significance1157803993157803993Humanname
407483151CV3438875single nucleotide variantNM_052938.5(FCRL1):c.265C>G (p.Gln89Glu)not specified [RCV004618518]uncertain significance1157803899157803899Humanname
597740006CV3676078single nucleotide variantNM_052938.5(FCRL1):c.188C>T (p.Pro63Leu)not specified [RCV004921373]likely benign1157803976157803976Humanname
598229655CV3959149single nucleotide variantNM_052938.5(FCRL1):c.224C>T (p.Ala75Val)not specified [RCV005342111]uncertain significance1157803940157803940Humanname
598229666CV3959151single nucleotide variantNM_052938.5(FCRL1):c.223G>C (p.Ala75Pro)not specified [RCV005342113]uncertain significance1157803941157803941Humanname
598229679CV3959153single nucleotide variantNM_052938.5(FCRL1):c.110C>G (p.Thr37Arg)not specified [RCV005342115]uncertain significance1157804054157804054Humanname
156102801CV2260455single nucleotide variantNM_052938.5(FCRL1):c.479C>T (p.Thr160Ile)not specified [RCV004123250]uncertain significance1157802505157802505Humanname
156291810CV2321156single nucleotide variantNM_052938.5(FCRL1):c.880T>C (p.Phe294Leu)not specified [RCV004175282]uncertain significance1157801921157801921Humanname
329356695CV2460482single nucleotide variantNM_052938.5(FCRL1):c.334G>A (p.Asp112Asn)not specified [RCV004268775]likely benign1157802650157802650Humanname
401772353CV2719615single nucleotide variantNM_052938.5(FCRL1):c.320G>C (p.Arg107Thr)not specified [RCV004327282]uncertain significance1157802664157802664Humanname
405742347CV3256911single nucleotide variantNM_052938.5(FCRL1):c.753C>G (p.Ser251Arg)not specified [RCV004391527]uncertain significance1157802048157802048Humanname
405742356CV3256912single nucleotide variantNM_052938.5(FCRL1):c.764C>A (p.Pro255His)not specified [RCV004391528]uncertain significance1157802037157802037Humanname
407483134CV3438872single nucleotide variantNM_052938.5(FCRL1):c.668A>G (p.Asp223Gly)not specified [RCV004618515]uncertain significance1157802133157802133Humanname
407483138CV3438873single nucleotide variantNM_052938.5(FCRL1):c.670G>A (p.Val224Met)not specified [RCV004618516]uncertain significance1157802131157802131Humanname
597739962CV3676069single nucleotide variantNM_052938.5(FCRL1):c.760G>C (p.Ala254Pro)not specified [RCV004921364]uncertain significance1157802041157802041Humanname
597739967CV3676070single nucleotide variantNM_052938.5(FCRL1):c.931G>A (p.Glu311Lys)not specified [RCV004921365]uncertain significance1157801533157801533Humanname
597739983CV3676073single nucleotide variantNM_052938.5(FCRL1):c.397A>G (p.Ile133Val)not specified [RCV004921368]likely benign1157802587157802587Humanname
597739988CV3676074single nucleotide variantNM_052938.5(FCRL1):c.508A>C (p.Ile170Leu)not specified [RCV004921369]uncertain significance1157802476157802476Humanname
597739992CV3676075single nucleotide variantNM_052938.5(FCRL1):c.766T>G (p.Ser256Ala)not specified [RCV004921370]uncertain significance1157802035157802035Humanname
597739997CV3676076single nucleotide variantNM_052938.5(FCRL1):c.691G>A (p.Ala231Thr)not specified [RCV004921371]uncertain significance1157802110157802110Humanname
597740002CV3676077single nucleotide variantNM_052938.5(FCRL1):c.856C>A (p.Arg286Ser)not specified [RCV004921372]uncertain significance1157801945157801945Humanname
598229649CV3959148single nucleotide variantNM_052938.5(FCRL1):c.967G>A (p.Ala323Thr)not specified [RCV005342110]uncertain significance1157801497157801497Humanname
598229661CV3959150single nucleotide variantNM_052938.5(FCRL1):c.737A>C (p.Asp246Ala)not specified [RCV005342112]uncertain significance1157802064157802064Humanname
156185472CV2292323single nucleotide variantNM_052938.5(FCRL1):c.1069C>A (p.Leu357Ile)not specified [RCV004150140]uncertain significance1157798206157798206Humanname
156340199CV2363198single nucleotide variantNM_052938.5(FCRL1):c.1004G>A (p.Gly335Glu)not specified [RCV004213765]uncertain significance1157800085157800085Humanname
329357713CV2453759single nucleotide variantNM_052938.5(FCRL1):c.1133A>G (p.Asp378Gly)not specified [RCV004269386]uncertain significance1157797921157797921Humanname
401773393CV2698197single nucleotide variantNM_052938.5(FCRL1):c.1079C>T (p.Pro360Leu)not specified [RCV004304764]uncertain significance1157798196157798196Humanname
401763623CV2714620single nucleotide variantNM_052938.5(FCRL1):c.1261A>G (p.Thr421Ala)not specified [RCV004318113]uncertain significance1157796128157796128Humanname
405742330CV3256908single nucleotide variantNM_052938.5(FCRL1):c.1201A>T (p.Thr401Ser)not specified [RCV004391524]uncertain significance1157797118157797118Humanname
597739973CV3676071single nucleotide variantNM_052938.5(FCRL1):c.1252G>A (p.Ala418Thr)not specified [RCV004921366]uncertain significance1157796137157796137Humanname
597739978CV3676072single nucleotide variantNM_052938.5(FCRL1):c.1160A>C (p.Asn387Thr)not specified [RCV004921367]uncertain significance1157797894157797894Humanname
8624741CV79855single nucleotide variantNM_001159397.1(FCRL1):c.741C>T (p.Ile247=)Malignant melanoma [RCV000059931]not provided1157802060157802060Humanname
8628994CV84137single nucleotide variantNM_001159397.1(FCRL1):c.945C>T (p.Phe315=)Malignant melanoma [RCV000064218]not provided1157798213157798213Humanname
8624740CV79854single nucleotide variantNM_001159397.1(FCRL1):c.841G>A (p.Gly281Ser)Malignant melanoma [RCV000059930]not provided1157801960157801960Humanname
8628995CV84138single nucleotide variantNM_001159397.1(FCRL1):c.904G>A (p.Asp302Asn)Malignant melanoma [RCV000064219]not provided1157800068157800068Humanname
8628996CV84139single nucleotide variantNM_001159397.1(FCRL1):c.556G>A (p.Glu186Lys)Malignant melanoma [RCV000064220]not provided1157802428157802428Humanname