Tcea2 Variant Search Result - Rat Genome Database

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21 records found for search term Tcea2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8586615	CV121219	single nucleotide variant	NM_198723.1(TCEA2):c.-244G>T	Lung cancer [RCV000101739]	uncertain significance	20	64057491	64057491	Human		name
8637440	CV92666	single nucleotide variant	NM_198723.1(TCEA2):c.222G>A (p.Arg74=)	Malignant melanoma [RCV000072764]	not provided	20	64068108	64068108	Human		name
401882363	CV2793464	single nucleotide variant	NM_003195.6(TCEA2):c.94C>T (p.Arg32Trp)	not specified [RCV004362551]	uncertain significance	20	64066497	64066497	Human		name
156211786	CV2378334	single nucleotide variant	NM_003195.6(TCEA2):c.107C>G (p.Ala36Gly)	not specified [RCV004226361]	uncertain significance	20	64066510	64066510	Human		name
405745841	CV3331739	single nucleotide variant	NM_003195.6(TCEA2):c.269G>A (p.Arg90Gln)	not specified [RCV004466370]	likely benign	20	64068074	64068074	Human		name
407530749	CV3485813	single nucleotide variant	NM_003195.6(TCEA2):c.293C>T (p.Thr98Met)	not specified [RCV004682070]	uncertain significance	20	64068098	64068098	Human		name
156296478	CV2297578	single nucleotide variant	NM_003195.6(TCEA2):c.332G>T (p.Arg111Leu)	not specified [RCV004155281]	uncertain significance	20	64069363	64069363	Human		name
156116730	CV2349409	single nucleotide variant	NM_003195.6(TCEA2):c.469G>A (p.Val157Met)	not specified [RCV004199339]	uncertain significance	20	64069773	64069773	Human		name
156068436	CV2356854	single nucleotide variant	NM_003195.6(TCEA2):c.751A>G (p.Thr251Ala)	not specified [RCV004204232]	uncertain significance	20	64070567	64070567	Human		name
329399263	CV2470015	single nucleotide variant	NM_003195.6(TCEA2):c.307G>A (p.Ala103Thr)	not specified [RCV004287291]	uncertain significance	20	64068112	64068112	Human		name
401721821	CV2680689	single nucleotide variant	NM_003195.6(TCEA2):c.467A>G (p.His156Arg)	not specified [RCV004291302]	uncertain significance	20	64069771	64069771	Human		name
401744676	CV2688210	single nucleotide variant	NM_003195.6(TCEA2):c.857T>A (p.Phe286Tyr)	not specified [RCV004298901]	uncertain significance	20	64071907	64071907	Human		name
401731671	CV2693939	single nucleotide variant	NM_003195.6(TCEA2):c.442G>A (p.Ala148Thr)	not specified [RCV004300234]	uncertain significance	20	64069473	64069473	Human		name
401729317	CV2732956	single nucleotide variant	NM_003195.6(TCEA2):c.389C>T (p.Pro130Leu)	not specified [RCV004331133]	uncertain significance	20	64069420	64069420	Human		name
405745854	CV3331741	single nucleotide variant	NM_003195.6(TCEA2):c.336G>T (p.Lys112Asn)	not specified [RCV004466372]	uncertain significance	20	64069367	64069367	Human		name
405745862	CV3331742	single nucleotide variant	NM_003195.6(TCEA2):c.510C>G (p.Ile170Met)	not specified [RCV004466373]	uncertain significance	20	64069814	64069814	Human		name
407513060	CV3485814	single nucleotide variant	NM_003195.6(TCEA2):c.752C>A (p.Thr251Asn)	not specified [RCV004673598]	uncertain significance	20	64070568	64070568	Human		name
597771858	CV3619522	single nucleotide variant	NM_003195.6(TCEA2):c.490G>C (p.Glu164Gln)	not specified [RCV004871731]	likely benign	20	64069794	64069794	Human		name
598163451	CV3913163	single nucleotide variant	NM_003195.6(TCEA2):c.472G>A (p.Ala158Thr)	not specified [RCV005283124]	uncertain significance	20	64069776	64069776	Human		name
598209155	CV3913164	single nucleotide variant	NM_003195.6(TCEA2):c.455C>T (p.Thr152Met)	not specified [RCV005291642]	uncertain significance	20	64069486	64069486	Human		name
598209159	CV3913165	single nucleotide variant	NM_003195.6(TCEA2):c.704G>A (p.Arg235His)	not specified [RCV005291643]	uncertain significance	20	64070520	64070520	Human		name

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