Tmem33 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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13 records found for search term Tmem33

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401759278	CV2690849	single nucleotide variant	NM_018126.3(TMEM33):c.81G>A (p.Met27Ile)	not specified [RCV004298554]	uncertain significance	4	41938637	41938637	Human		name
405755736	CV3346502	single nucleotide variant	NM_018126.3(TMEM33):c.57G>C (p.Met19Ile)	not specified [RCV004467793]	uncertain significance	4	41938613	41938613	Human		name
407526681	CV3482724	single nucleotide variant	NM_018126.3(TMEM33):c.35C>G (p.Ala12Gly)	not specified [RCV004679727]	uncertain significance	4	41935519	41935519	Human		name
407526688	CV3482726	single nucleotide variant	NM_018126.3(TMEM33):c.52A>G (p.Met18Val)	not specified [RCV004679729]	uncertain significance	4	41938608	41938608	Human		name
407526692	CV3482727	single nucleotide variant	NM_018126.3(TMEM33):c.86T>G (p.Leu29Arg)	not specified [RCV004679730]	uncertain significance	4	41938642	41938642	Human		name
598226839	CV3913891	single nucleotide variant	NM_018126.3(TMEM33):c.28C>A (p.Gln10Lys)	not specified [RCV005294487]	uncertain significance	4	41935512	41935512	Human		name
156161590	CV2272608	single nucleotide variant	NM_018126.3(TMEM33):c.100A>G (p.Thr34Ala)	not specified [RCV004133489]	uncertain significance	4	41938656	41938656	Human		name
156134766	CV2284685	single nucleotide variant	NM_018126.3(TMEM33):c.104T>C (p.Val35Ala)	not specified [RCV004140838]	uncertain significance	4	41938660	41938660	Human		name
155940703	CV2294123	single nucleotide variant	NM_018126.3(TMEM33):c.134T>C (p.Leu45Pro)	not specified [RCV004149493]	uncertain significance	4	41938690	41938690	Human		name
407526685	CV3482725	single nucleotide variant	NM_018126.3(TMEM33):c.244G>A (p.Ala82Thr)	not specified [RCV004679728]	uncertain significance	4	41939299	41939299	Human		name
156165676	CV2348616	single nucleotide variant	NM_018126.3(TMEM33):c.578C>T (p.Thr193Ile)	not specified [RCV004195841]	uncertain significance	4	41949349	41949349	Human		name
407526677	CV3482723	single nucleotide variant	NM_018126.3(TMEM33):c.590C>T (p.Ser197Leu)	not specified [RCV004679726]	uncertain significance	4	41949361	41949361	Human		name
598226831	CV3913890	single nucleotide variant	NM_018126.3(TMEM33):c.596G>A (p.Arg199Gln)	not specified [RCV005294486]	uncertain significance	4	41949367	41949367	Human		name