Tm2d2 Variant Search Result - Rat Genome Database

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21 records found for search term Tm2d2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405784092	CV3342993	single nucleotide variant	NM_078473.3(TM2D2):c.23T>C (p.Val8Ala)	not specified [RCV004472478]	uncertain significance	8	38996417	38996417	Human		name
401855944	CV2754129	single nucleotide variant	NM_078473.3(TM2D2):c.67A>G (p.Asn23Asp)	not specified [RCV004334325]	uncertain significance	8	38996373	38996373	Human		name
405784108	CV3342996	single nucleotide variant	NM_078473.3(TM2D2):c.34C>T (p.Leu12Phe)	not specified [RCV004472481]	uncertain significance	8	38996406	38996406	Human		name
598199929	CV3920782	single nucleotide variant	NM_078473.3(TM2D2):c.97A>G (p.Ser33Gly)	not specified [RCV005289918]	uncertain significance	8	38996343	38996343	Human		name
156116558	CV2209096	single nucleotide variant	NM_078473.3(TM2D2):c.145G>C (p.Ala49Pro)	not specified [RCV004093326]	uncertain significance	8	38996295	38996295	Human		name
156114265	CV2225062	single nucleotide variant	NM_078473.3(TM2D2):c.179G>A (p.Ser60Asn)	not specified [RCV004094884]	likely benign	8	38996261	38996261	Human		name
155951953	CV2309856	single nucleotide variant	NM_078473.3(TM2D2):c.269T>C (p.Val90Ala)	not specified [RCV004160965]	uncertain significance	8	38995364	38995364	Human		name
156343339	CV2364098	single nucleotide variant	NM_078473.3(TM2D2):c.155C>T (p.Pro52Leu)	not specified [RCV004221479]	uncertain significance	8	38996285	38996285	Human		name
156003275	CV2399644	single nucleotide variant	NM_078473.3(TM2D2):c.148G>T (p.Ala50Ser)	not specified [RCV004244160]	uncertain significance	8	38996292	38996292	Human		name
401758643	CV2700667	single nucleotide variant	NM_078473.3(TM2D2):c.130C>G (p.Leu44Val)	not specified [RCV004313384]	uncertain significance	8	38996310	38996310	Human		name
401880113	CV2783098	single nucleotide variant	NM_078473.3(TM2D2):c.214C>T (p.Leu72Phe)	not specified [RCV004363453]	uncertain significance	8	38996226	38996226	Human		name
405784087	CV3342992	single nucleotide variant	NM_078473.3(TM2D2):c.206C>T (p.Pro69Leu)	not specified [RCV004472477]	uncertain significance	8	38996234	38996234	Human		name
405784098	CV3342994	single nucleotide variant	NM_078473.3(TM2D2):c.283G>A (p.Ala95Thr)	not specified [RCV004472479]	uncertain significance	8	38995350	38995350	Human		name
407452735	CV3475968	single nucleotide variant	NM_078473.3(TM2D2):c.134C>T (p.Thr45Ile)	not specified [RCV004684193]	uncertain significance	8	38996306	38996306	Human		name
597775920	CV3620052	single nucleotide variant	NM_078473.3(TM2D2):c.221C>T (p.Ser74Phe)	not specified [RCV004872662]	uncertain significance	8	38996219	38996219	Human		name
155904786	CV2298864	single nucleotide variant	NM_078473.3(TM2D2):c.376G>A (p.Gly126Arg)	not specified [RCV004156408]	uncertain significance	8	38993600	38993600	Human		name
156105300	CV2352522	single nucleotide variant	NM_078473.3(TM2D2):c.439G>A (p.Gly147Arg)	not specified [RCV004203024]	uncertain significance	8	38991538	38991538	Human		name
155935176	CV2371741	single nucleotide variant	NM_078473.3(TM2D2):c.383A>G (p.Glu128Gly)	not specified [RCV004219409]	uncertain significance	8	38993593	38993593	Human		name
405784102	CV3342995	single nucleotide variant	NM_078473.3(TM2D2):c.319G>A (p.Gly107Ser)	not specified [RCV004472480]	uncertain significance	8	38993657	38993657	Human		name
407452737	CV3475969	single nucleotide variant	NM_078473.3(TM2D2):c.451A>G (p.Ile151Val)	not specified [RCV004684194]	uncertain significance	8	38991526	38991526	Human		name
598177302	CV3920783	single nucleotide variant	NM_078473.3(TM2D2):c.412G>A (p.Glu138Lys)	not specified [RCV005285797]	uncertain significance	8	38993564	38993564	Human		name

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