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5 records found for search term Tmem191c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156240310CV2245967single nucleotide variantNM_001388354.1(TMEM191C):c.-24C>Tnot specified [RCV004113896]uncertain significance222146743621467436Humanname
156279839CV2338345single nucleotide variantNM_001388354.1(TMEM191C):c.525+5G>Anot specified [RCV004186396]uncertain significance222146900821469008Humanname
155959161CV2193759single nucleotide variantNM_001388354.1(TMEM191C):c.2T>C (p.Met1Thr)not specified [RCV004074521]uncertain significance222146746121467461Humanname
155971507CV2334224single nucleotide variantNM_001388354.1(TMEM191C):c.62G>A (p.Arg21Gln)not specified [RCV004186208]uncertain significance222146752121467521Humanname
155920341CV2240347single nucleotide variantNM_001388354.1(TMEM191C):c.656C>A (p.Ala219Glu)not specified [RCV004117252]uncertain significance222146933921469339Humanname