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53 records found for search term Brd7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401732910CV2705080single nucleotide variantNM_013263.5(BRD7):c.5G>A (p.Gly2Asp)not specified [RCV004309991]uncertain significance165036877050368770Humanname
405765173CV3302130single nucleotide variantNM_013263.5(BRD7):c.15C>A (p.His5Gln)not specified [RCV004434313]uncertain significance165036876050368760Humanname
597749375CV3637022single nucleotide variantNM_013263.5(BRD7):c.39C>A (p.His13Gln)not specified [RCV004892343]uncertain significance165036873650368736Humanname
156112122CV2218010single nucleotide variantNM_013263.5(BRD7):c.162T>A (p.Asp54Glu)not specified [RCV004086456]uncertain significance165036818650368186Humanname
156336439CV2360735single nucleotide variantNM_013263.5(BRD7):c.287G>A (p.Arg96Gln)not specified [RCV004213521]uncertain significance165035489450354894Humanname
401769642CV2689868single nucleotide variantNM_013263.5(BRD7):c.136T>C (p.Ser46Pro)not specified [RCV004297766]uncertain significance165036821250368212Humanname
401911667CV2807922single nucleotide variantNM_013263.5(BRD7):c.147C>G (p.Phe49Leu)not provided [RCV003426698]likely benign165036820150368201Humanname
405765180CV3302131single nucleotide variantNM_013263.5(BRD7):c.215A>G (p.Gln72Arg)not specified [RCV004434314]uncertain significance165036813350368133Humanname
405765187CV3302132single nucleotide variantNM_013263.5(BRD7):c.296A>G (p.Asn99Ser)not specified [RCV004434315]uncertain significance165035488550354885Humanname
407481328CV3421380single nucleotide variantNM_013263.5(BRD7):c.158A>T (p.Asn53Ile)not specified [RCV004602452]uncertain significance165036819050368190Humanname
597783284CV3637014single nucleotide variantNM_013263.5(BRD7):c.251G>A (p.Arg84Lys)not specified [RCV004900230]uncertain significance165036809750368097Humanname
597783292CV3637016single nucleotide variantNM_013263.5(BRD7):c.233A>G (p.Lys78Arg)not specified [RCV004900232]uncertain significance165036811550368115Humanname
597783302CV3637020single nucleotide variantNM_013263.5(BRD7):c.220C>T (p.Pro74Ser)not specified [RCV004900234]uncertain significance165036812850368128Humanname
597783321CV3637026single nucleotide variantNM_013263.5(BRD7):c.127G>A (p.Gly43Arg)not specified [RCV004900239]uncertain significance165036822150368221Humanname
598173660CV3938889single nucleotide variantNM_013263.5(BRD7):c.206G>A (p.Gly69Glu)not specified [RCV005309589]uncertain significance165036814250368142Humanname
598173666CV3938891single nucleotide variantNM_013263.5(BRD7):c.188G>C (p.Arg63Pro)not specified [RCV005309590]uncertain significance165036816050368160Humanname
156154175CV2242259single nucleotide variantNM_013263.5(BRD7):c.406C>G (p.Leu136Val)not specified [RCV004111283]uncertain significance165035446550354465Humanname
155981360CV2244067single nucleotide variantNM_013263.5(BRD7):c.305A>G (p.Glu102Gly)not specified [RCV004108546]uncertain significance165035487650354876Humanname
156272365CV2283576single nucleotide variantNM_013263.5(BRD7):c.423T>A (p.Asn141Lys)not specified [RCV004140088]uncertain significance165035444850354448Humanname
156395929CV2326002single nucleotide variantNM_013263.5(BRD7):c.373T>A (p.Leu125Ile)not specified [RCV004176213]uncertain significance165035480850354808Humanname
155983722CV2367813single nucleotide variantNM_013263.5(BRD7):c.391G>A (p.Val131Ile)not specified [RCV004222927]uncertain significance165035448050354480Humanname
156153137CV2394929single nucleotide variantNM_013263.5(BRD7):c.319T>C (p.Cys107Arg)not specified [RCV004234579]uncertain significance165035486250354862Humanname
401747237CV2698818single nucleotide variantNM_013263.5(BRD7):c.827G>T (p.Arg276Ile)not specified [RCV004301260]uncertain significance165033477150334771Humanname
401864835CV2757219single nucleotide variantNM_013263.5(BRD7):c.513C>G (p.Ile171Met)not specified [RCV004338817]uncertain significance165035010150350101Humanname
405765194CV3302133single nucleotide variantNM_013263.5(BRD7):c.983A>G (p.Lys328Arg)not specified [RCV004434316]uncertain significance165033360250333602Humanname
407500512CV3421377single nucleotide variantNM_013263.5(BRD7):c.347C>T (p.Pro116Leu)not specified [RCV004607147]uncertain significance165035483450354834Humanname
597783289CV3637015single nucleotide variantNM_013263.5(BRD7):c.767A>G (p.Gln256Arg)not specified [RCV004900231]uncertain significance165033483150334831Humanname
597783296CV3637018single nucleotide variantNM_013263.5(BRD7):c.508A>G (p.Met170Val)not specified [RCV004900233]uncertain significance165035010650350106Humanname
597783313CV3637024single nucleotide variantNM_013263.5(BRD7):c.383A>G (p.Gln128Arg)not specified [RCV004900237]uncertain significance165035479850354798Humanname
597783317CV3637025single nucleotide variantNM_013263.5(BRD7):c.952C>G (p.Leu318Val)not specified [RCV004900238]uncertain significance165033363350333633Humanname
10398714CV204463single nucleotide variantNM_013263.5(BRD7):c.1834C>T (p.Arg612Ter)Granular cell cancer [RCV000190398]likely pathogenic165031995350319953Human1name
156246052CV2263692single nucleotide variantNM_013263.5(BRD7):c.1415A>T (p.His472Leu)not specified [RCV004135987]uncertain significance165032361550323615Humanname
156082796CV2301197single nucleotide variantNM_013263.5(BRD7):c.1792C>G (p.Gln598Glu)not specified [RCV004160105]uncertain significance165031999550319995Humanname
156067742CV2320287single nucleotide variantNM_013263.5(BRD7):c.1385G>C (p.Ser462Thr)not specified [RCV004178455]uncertain significance165032364550323645Humanname
156078419CV2341186single nucleotide variantNM_013263.5(BRD7):c.1510G>A (p.Val504Ile)not specified [RCV004186607]likely benign165032076550320765Humanname
156208928CV2370049single nucleotide variantNM_013263.5(BRD7):c.1246T>A (p.Ser416Thr)not specified [RCV004210945]uncertain significance165032583350325833Humanname
401731330CV2701314single nucleotide variantNM_013263.5(BRD7):c.1748T>A (p.Met583Lys)not specified [RCV004311691]uncertain significance165032025650320256Humanname
401879416CV2755087single nucleotide variantNM_013263.5(BRD7):c.1528T>G (p.Leu510Val)not specified [RCV004335240]uncertain significance165032074750320747Humanname
401892101CV2777231single nucleotide variantNM_013263.5(BRD7):c.1559C>T (p.Ala520Val)not specified [RCV004354261]uncertain significance165032071650320716Humanname
405765156CV3302127single nucleotide variantNM_013263.5(BRD7):c.1102C>T (p.Pro368Ser)not specified [RCV004434310]uncertain significance165032637750326377Humanname
405765162CV3302128single nucleotide variantNM_013263.5(BRD7):c.1186G>A (p.Val396Ile)not specified [RCV004434311]uncertain significance165032629350326293Humanname
405765168CV3302129single nucleotide variantNM_013263.5(BRD7):c.1477C>G (p.Leu493Val)not specified [RCV004434312]uncertain significance165032200550322005Humanname
407481321CV3421378single nucleotide variantNM_013263.5(BRD7):c.1730G>A (p.Gly577Asp)not specified [RCV004602451]uncertain significance165032027450320274Humanname
407481337CV3421381single nucleotide variantNM_013263.5(BRD7):c.1762C>G (p.Gln588Glu)not specified [RCV004602453]uncertain significance165032002550320025Humanname
407481343CV3421382single nucleotide variantNM_013263.5(BRD7):c.1771A>G (p.Asn591Asp)not specified [RCV004602454]uncertain significance165032001650320016Humanname
407500520CV3421383single nucleotide variantNM_013263.5(BRD7):c.1675G>A (p.Ala559Thr)not specified [RCV004607149]uncertain significance165032032950320329Humanname
407481352CV3421384single nucleotide variantNM_013263.5(BRD7):c.1484C>A (p.Thr495Lys)not specified [RCV004602455]uncertain significance165032199850321998Humanname
597749369CV3637017single nucleotide variantNM_013263.5(BRD7):c.1865C>T (p.Pro622Leu)not specified [RCV004892342]uncertain significance165031992250319922Humanname
597783304CV3637021single nucleotide variantNM_013263.5(BRD7):c.1010A>G (p.Gln337Arg)not specified [RCV004900235]uncertain significance165033357550333575Humanname
597783309CV3637023single nucleotide variantNM_013263.5(BRD7):c.1465C>G (p.His489Asp)not specified [RCV004900236]uncertain significance165032201750322017Humanname
597783324CV3637027single nucleotide variantNM_013263.5(BRD7):c.1115G>A (p.Gly372Glu)not specified [RCV004900240]uncertain significance165032636450326364Humanname
598173647CV3938887single nucleotide variantNM_013263.5(BRD7):c.1585G>A (p.Val529Ile)not specified [RCV005309587]uncertain significance165032069050320690Humanname
598210750CV3938890single nucleotide variantNM_013263.5(BRD7):c.1816G>C (p.Val606Leu)not specified [RCV005315909]uncertain significance165031997150319971Humanname