Tmem97 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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9 records found for search term Tmem97

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329359038	CV2450810	single nucleotide variant	NM_014573.3(TMEM97):c.147G>C (p.Trp49Cys)	not specified [RCV004267727]	uncertain significance	17	28325523	28325523	Human		name
401783036	CV2716098	single nucleotide variant	NM_014573.3(TMEM97):c.179A>G (p.Gln60Arg)	not specified [RCV004323342]	uncertain significance	17	28325555	28325555	Human		name
405772879	CV3343370	single nucleotide variant	NM_014573.3(TMEM97):c.107G>T (p.Arg36Leu)	not specified [RCV004470597]	uncertain significance	17	28319346	28319346	Human		name
597800824	CV3610782	single nucleotide variant	NM_014573.3(TMEM97):c.187C>T (p.Pro63Ser)	not specified [RCV004880410]	uncertain significance	17	28325563	28325563	Human		name
401736652	CV2688845	single nucleotide variant	NM_014573.3(TMEM97):c.364G>A (p.Asp122Asn)	not specified [RCV004303861]	uncertain significance	17	28326626	28326626	Human		name
405772885	CV3343371	single nucleotide variant	NM_014573.3(TMEM97):c.411G>C (p.Leu137Phe)	not specified [RCV004470598]	likely benign	17	28326673	28326673	Human		name
405772890	CV3343372	single nucleotide variant	NM_014573.3(TMEM97):c.419G>A (p.Arg140Gln)	not specified [RCV004470599]	uncertain significance	17	28326681	28326681	Human		name
597800820	CV3610780	single nucleotide variant	NM_014573.3(TMEM97):c.337C>T (p.Pro113Ser)	not specified [RCV004880408]	uncertain significance	17	28326599	28326599	Human		name
597800822	CV3610781	single nucleotide variant	NM_014573.3(TMEM97):c.482T>A (p.Met161Lys)	not specified [RCV004880409]	uncertain significance	17	28326744	28326744	Human		name