Trim39 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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15 records found for search term Trim39

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156252789	CV2283992	single nucleotide variant	NM_001369521.2(TRIM39):c.804-226C>T	not specified [RCV004144610]	likely benign	6	30340279	30340279	Human		name
156262260	CV2319774	single nucleotide variant	NM_001369521.2(TRIM39):c.804-187C>T	not specified [RCV004187306]	uncertain significance	6	30340318	30340318	Human		name
401860339	CV2762401	single nucleotide variant	NM_001369521.2(TRIM39):c.804-232A>C	not specified [RCV004335507]	likely benign	6	30340273	30340273	Human		name
405790339	CV3336960	single nucleotide variant	NM_001369521.2(TRIM39):c.804-172C>T	not specified [RCV004473839]	likely benign	6	30340333	30340333	Human		name
598274149	CV3935450	single nucleotide variant	NM_001369521.2(TRIM39):c.804-194C>G	not specified [RCV005303783]	uncertain significance	6	30340311	30340311	Human		name
8581848	CV116293	single nucleotide variant	NM_001199119.1(TRIM39-RPP21):c.1288+128C>T	Lung cancer [RCV000096816]	uncertain significance	6	30345701	30345701	Human		name
8631970	CV87176	single nucleotide variant	NM_021253.3(TRIM39):c.1226T>C (p.Val409Ala)	Malignant melanoma [RCV000067267]	not provided	6	30341928	30341928	Human		name
156254723	CV2264673	single nucleotide variant	NM_001369521.2(TRIM39):c.1441A>G (p.Ile481Val)	not specified [RCV004132672]	uncertain significance	6	30342233	30342233	Human		name
156248552	CV2307239	single nucleotide variant	NM_001369521.2(TRIM39):c.1340G>A (p.Arg447His)	not specified [RCV004159700]	uncertain significance	6	30342132	30342132	Human		name
401763232	CV2707600	single nucleotide variant	NM_001369521.2(TRIM39):c.1150G>A (p.Val384Met)	not specified [RCV004306541]	uncertain significance	6	30341942	30341942	Human		name
405790335	CV3336959	single nucleotide variant	NM_001369521.2(TRIM39):c.1288A>G (p.Ile430Val)	not specified [RCV004473838]	likely benign	6	30342080	30342080	Human		name
597801780	CV3617738	single nucleotide variant	NM_001369521.2(TRIM39):c.1141C>T (p.Arg381Trp)	not specified [RCV004880900]	uncertain significance	6	30341933	30341933	Human		name
597801782	CV3617739	single nucleotide variant	NM_001369521.2(TRIM39):c.1142G>A (p.Arg381Gln)	not specified [RCV004880901]	likely benign	6	30341934	30341934	Human		name
598202676	CV3935449	single nucleotide variant	NM_001369521.2(TRIM39):c.1345C>T (p.His449Tyr)	not specified [RCV005290415]	uncertain significance	6	30342137	30342137	Human		name
405790341	CV3336961	single nucleotide variant	NM_001199119.1(TRIM39-RPP21):c.1031G>A (p.Arg344Lys)	not specified [RCV004473840]	uncertain significance	6	30341823	30341823	Human		name