Ttc9b Variant Search Result - Rat Genome Database

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12 records found for search term Ttc9b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156139388	CV2280743	single nucleotide variant	NM_152479.6(TTC9B):c.52C>A (p.Pro18Thr)	not specified [RCV004143193]	uncertain significance	19	40218330	40218330	Human		name
156369909	CV2263440	single nucleotide variant	NM_152479.6(TTC9B):c.269G>A (p.Arg90Gln)	not specified [RCV004133686]	uncertain significance	19	40218113	40218113	Human		name
401748820	CV2708362	single nucleotide variant	NM_152479.6(TTC9B):c.193G>A (p.Ala65Thr)	not specified [RCV004313480]	uncertain significance	19	40218189	40218189	Human		name
407531885	CV3487317	single nucleotide variant	NM_152479.6(TTC9B):c.101G>A (p.Gly34Asp)	not specified [RCV004682726]	uncertain significance	19	40218281	40218281	Human		name
597797189	CV3625553	single nucleotide variant	NM_152479.6(TTC9B):c.112C>T (p.Arg38Cys)	not specified [RCV004878764]	uncertain significance	19	40218270	40218270	Human		name
156269689	CV2326402	single nucleotide variant	NM_152479.6(TTC9B):c.469C>A (p.Arg157Ser)	not specified [RCV004182976]	uncertain significance	19	40217328	40217328	Human		name
329369718	CV2461196	single nucleotide variant	NM_152479.6(TTC9B):c.659G>A (p.Arg220His)	not specified [RCV004267393]	uncertain significance	19	40216224	40216224	Human		name
401879965	CV2783049	single nucleotide variant	NM_152479.6(TTC9B):c.592C>G (p.Arg198Gly)	not specified [RCV004363419]	uncertain significance	19	40217205	40217205	Human		name
405804521	CV3337646	single nucleotide variant	NM_152479.6(TTC9B):c.425C>G (p.Thr142Arg)	not specified [RCV004479294]	uncertain significance	19	40217957	40217957	Human		name
597797183	CV3625551	single nucleotide variant	NM_152479.6(TTC9B):c.565C>G (p.Arg189Gly)	not specified [RCV004878762]	uncertain significance	19	40217232	40217232	Human		name
597797186	CV3625552	single nucleotide variant	NM_152479.6(TTC9B):c.692G>A (p.Gly231Glu)	not specified [RCV004878763]	uncertain significance	19	40216191	40216191	Human		name
598253621	CV3925347	single nucleotide variant	NM_152479.6(TTC9B):c.607A>G (p.Thr203Ala)	not specified [RCV005299105]	uncertain significance	19	40217190	40217190	Human		name