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6 records found for search term Tmem167b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597753123CV3616945single nucleotide variantNM_020141.4(TMEM167B):c.16T>G (p.Ser6Ala)not specified [RCV004867306]uncertain significance1109092895109092895Humanname
401755780CV2679106single nucleotide variantNM_020141.4(TMEM167B):c.77A>C (p.Lys26Thr)not specified [RCV004295096]uncertain significance1109092956109092956Humanname
405794726CV3336063single nucleotide variantNM_020141.4(TMEM167B):c.72C>G (p.Phe24Leu)not specified [RCV004475308]uncertain significance1109092951109092951Humanname
597753116CV3616944single nucleotide variantNM_020141.4(TMEM167B):c.74A>G (p.Lys25Arg)not specified [RCV004867305]uncertain significance1109092953109092953Humanname
401865001CV2791445single nucleotide variantNM_020141.4(TMEM167B):c.130G>C (p.Val44Leu)not specified [RCV004358834]uncertain significance1109093009109093009Humanname
405794723CV3336062single nucleotide variantNM_020141.4(TMEM167B):c.193G>A (p.Val65Ile)not specified [RCV004475307]uncertain significance1109094467109094467Humanname