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30 records found for search term Tmem134
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401864836CV2791381single nucleotide variantNM_025124.4(TMEM134):c.7G>T (p.Ala3Ser)not specified [RCV004358783]uncertain significance116746918667469186Humanname
407458662CV3486376single nucleotide variantNM_025124.4(TMEM134):c.264C>T (p.Arg88=)not specified [RCV004686897]likely benign116746756667467566Humanname
597752651CV3616815single nucleotide variantNM_025124.4(TMEM134):c.23T>A (p.Phe8Tyr)not specified [RCV004867197]uncertain significance116746917067469170Humanname
156210949CV2306010single nucleotide variantNM_025124.4(TMEM134):c.61G>C (p.Gly21Arg)not specified [RCV004160997]uncertain significance116746913267469132Humanname
401753336CV2722434single nucleotide variantNM_025124.4(TMEM134):c.77A>T (p.Glu26Val)not specified [RCV004322829]uncertain significance116746911667469116Humanname
156274184CV2319972single nucleotide variantNM_025124.4(TMEM134):c.268T>C (p.Ser90Pro)not specified [RCV004167845]uncertain significance116746756267467562Humanname
155929851CV2389248single nucleotide variantNM_025124.4(TMEM134):c.169T>C (p.Tyr57His)not specified [RCV004235568]uncertain significance116746902467469024Humanname
329397737CV2456529single nucleotide variantNM_025124.4(TMEM134):c.272A>C (p.Gln91Pro)not specified [RCV004275669]uncertain significance116746755867467558Humanname
401782167CV2686569single nucleotide variantNM_025124.4(TMEM134):c.262C>T (p.Arg88Cys)not specified [RCV004300001]uncertain significance116746756867467568Humanname
401909527CV2813407single nucleotide variantNM_025124.4(TMEM134):c.250C>T (p.Arg84Ter)not provided [RCV003398040]likely benign116746758067467580Humanname
405794646CV3339747single nucleotide variantNM_025124.4(TMEM134):c.155A>G (p.Gln52Arg)not specified [RCV004475158]likely benign116746903867469038Humanname
405794533CV3339748single nucleotide variantNM_025124.4(TMEM134):c.173A>C (p.Gln58Pro)not specified [RCV004475159]uncertain significance116746902067469020Humanname
405794445CV3339749single nucleotide variantNM_025124.4(TMEM134):c.197G>A (p.Gly66Glu)not specified [RCV004475160]uncertain significance116746807067468070Humanname
597752657CV3616816single nucleotide variantNM_025124.4(TMEM134):c.103C>A (p.Pro35Thr)not specified [RCV004867198]uncertain significance116746909067469090Humanname
598178218CV3917366single nucleotide variantNM_025124.4(TMEM134):c.263G>A (p.Arg88His)not specified [RCV005285944]uncertain significance116746756767467567Humanname
156030829CV2202553single nucleotide variantNM_025124.4(TMEM134):c.457T>G (p.Ser153Ala)not specified [RCV004080837]uncertain significance116746485167464851Humanname
156273107CV2247571single nucleotide variantNM_025124.4(TMEM134):c.555C>A (p.Phe185Leu)not specified [RCV004108873]uncertain significance116746464767464647Humanname
156161152CV2323421single nucleotide variantNM_025124.4(TMEM134):c.499C>T (p.Pro167Ser)not specified [RCV004171813]uncertain significance116746480967464809Humanname
156335599CV2333550single nucleotide variantNM_025124.4(TMEM134):c.307C>T (p.Arg103Cys)not specified [RCV004190236]uncertain significance116746752367467523Humanname
156176592CV2374457single nucleotide variantNM_025124.4(TMEM134):c.479C>T (p.Pro160Leu)not specified [RCV004231966]uncertain significance116746482967464829Humanname
401726719CV2677320single nucleotide variantNM_025124.4(TMEM134):c.561C>A (p.Phe187Leu)not specified [RCV004295936]uncertain significance116746464167464641Humanname
401765662CV2683381single nucleotide variantNM_025124.4(TMEM134):c.539A>G (p.Lys180Arg)not specified [RCV004288152]uncertain significance116746466367464663Humanname
405794374CV3339750single nucleotide variantNM_025124.4(TMEM134):c.416T>C (p.Leu139Pro)not specified [RCV004475161]uncertain significance116746509167465091Humanname
405794225CV3339752single nucleotide variantNM_025124.4(TMEM134):c.524T>G (p.Ile175Ser)not specified [RCV004475163]uncertain significance116746467867464678Humanname
405794173CV3339753single nucleotide variantNM_025124.4(TMEM134):c.579C>G (p.Phe193Leu)not specified [RCV004475164]uncertain significance116746462367464623Humanname
407453282CV3486378single nucleotide variantNM_025124.4(TMEM134):c.379T>G (p.Ser127Ala)not specified [RCV004684478]uncertain significance116746733967467339Humanname
407453284CV3486379single nucleotide variantNM_025124.4(TMEM134):c.383T>C (p.Phe128Ser)not specified [RCV004684479]uncertain significance116746733567467335Humanname
598212914CV3917367single nucleotide variantNM_025124.4(TMEM134):c.475G>C (p.Val159Leu)not specified [RCV005292221]uncertain significance116746483367464833Humanname
598212921CV3917368single nucleotide variantNM_025124.4(TMEM134):c.308G>A (p.Arg103His)not specified [RCV005292222]uncertain significance116746752267467522Humanname
598212935CV3917370single nucleotide variantNM_025124.4(TMEM134):c.517A>G (p.Ile173Val)not specified [RCV005292224]uncertain significance116746468567464685Humanname