Rdh8 Variant Search Result - Rat Genome Database

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18 records found for search term Rdh8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407459052	CV3465198	single nucleotide variant	NM_015725.4(RDH8):c.-8G>A	not specified [RCV004658013]	uncertain significance	19	10013490	10013490	Human		name
15148191	CV716108	single nucleotide variant	NM_015725.4(RDH8):c.237T>C (p.Cys79=)	not provided [RCV000967495]	benign	19	10017190	10017190	Human		name
597685948	CV3582979	single nucleotide variant	NM_015725.2(RDH8):c.34G>A (p.Gly12Ser)	not specified [RCV004849845]	uncertain significance	19	10013471	10013471	Human		name
15136268	CV716107	single nucleotide variant	NM_015725.4(RDH8):c.80A>G (p.His27Arg)	not provided [RCV000965426]	benign	19	10013577	10013577	Human		name
15136275	CV716109	single nucleotide variant	NM_015725.4(RDH8):c.411C>T (p.Ile137=)	not provided [RCV000965427]	benign	19	10018879	10018879	Human		name
329359699	CV2462189	single nucleotide variant	NM_015725.4(RDH8):c.274G>C (p.Gly92Arg)	not specified [RCV004266199]	uncertain significance	19	10018742	10018742	Human		name
329353235	CV2469020	single nucleotide variant	NM_015725.4(RDH8):c.274G>A (p.Gly92Arg)	not specified [RCV004274271]	uncertain significance	19	10018742	10018742	Human		name
405682845	CV3319457	single nucleotide variant	NM_015725.4(RDH8):c.253G>C (p.Asp85His)	not specified [RCV004443725]	uncertain significance	19	10017206	10017206	Human		name
597764719	CV3582980	single nucleotide variant	NM_015725.4(RDH8):c.109G>C (p.Ala37Pro)	not specified [RCV004849846]	uncertain significance	19	10017062	10017062	Human		name
597764729	CV3582982	single nucleotide variant	NM_015725.4(RDH8):c.223C>G (p.Gln75Glu)	not specified [RCV004849848]	uncertain significance	19	10017176	10017176	Human		name
329395078	CV2457847	single nucleotide variant	NM_015725.4(RDH8):c.718C>T (p.Gln240Ter)	not specified [RCV004269657]	uncertain significance	19	10021436	10021436	Human		name
401875102	CV2756227	single nucleotide variant	NM_015725.4(RDH8):c.860G>A (p.Arg287His)	not specified [RCV004338323]	uncertain significance	19	10021673	10021673	Human		name
405682848	CV3319458	single nucleotide variant	NM_015725.4(RDH8):c.799C>T (p.Leu267Phe)	not specified [RCV004443726]	uncertain significance	19	10021612	10021612	Human		name
407459064	CV3465196	single nucleotide variant	NM_015725.4(RDH8):c.551A>C (p.Glu184Ala)	not specified [RCV004658011]	uncertain significance	19	10021269	10021269	Human		name
597764715	CV3582978	single nucleotide variant	NM_015725.4(RDH8):c.631G>A (p.Glu211Lys)	not specified [RCV004849844]	uncertain significance	19	10021349	10021349	Human		name
598255660	CV3909016	single nucleotide variant	NM_015725.4(RDH8):c.377T>G (p.Leu126Arg)	not specified [RCV005259944]	uncertain significance	19	10018845	10018845	Human		name
15181066	CV716110	single nucleotide variant	NM_015725.4(RDH8):c.917C>T (p.Thr306Met)	not provided [RCV000974302]	benign	19	10021730	10021730	Human		name
15190191	CV727833	single nucleotide variant	NM_015725.4(RDH8):c.464A>T (p.Tyr155Phe)	not provided [RCV000888032]	likely benign	19	10020730	10020730	Human		name