Psmg4 Variant Search Result - Rat Genome Database

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17 records found for search term Psmg4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156262678	CV2226958	single nucleotide variant	NM_001128591.2(PSMG4):c.250+468G>A	not specified [RCV004097354]	uncertain significance	6	3264227	3264227	Human		name
155984107	CV2348200	single nucleotide variant	NM_001128591.2(PSMG4):c.250+488G>A	not specified [RCV004190842]	likely benign	6	3264247	3264247	Human		name
405672153	CV3378657	single nucleotide variant	NM_001128591.2(PSMG4):c.250+463G>C	not specified [RCV004515409]	uncertain significance	6	3264222	3264222	Human		name
597750450	CV3592179	single nucleotide variant	NM_001128591.2(PSMG4):c.250+540C>A	not specified [RCV004846462]	uncertain significance	6	3264299	3264299	Human		name
407531801	CV3471961	single nucleotide variant	NM_001128591.2(PSMG4):c.17T>C (p.Val6Ala)	not specified [RCV004657791]	likely benign	6	3259039	3259039	Human		name
156312835	CV2256931	single nucleotide variant	NM_001128591.2(PSMG4):c.52A>G (p.Ser18Gly)	not specified [RCV004121127]	uncertain significance	6	3259074	3259074	Human		name
156074650	CV2331681	single nucleotide variant	NM_001128591.2(PSMG4):c.88G>A (p.Val30Ile)	not specified [RCV004184311]	uncertain significance	6	3259110	3259110	Human		name
405672157	CV3378658	single nucleotide variant	NM_001128591.2(PSMG4):c.68A>G (p.Glu23Gly)	not specified [RCV004515410]	uncertain significance	6	3259090	3259090	Human		name
598171130	CV3908237	single nucleotide variant	NM_001128591.2(PSMG4):c.94C>G (p.Arg32Gly)	not specified [RCV005263275]	uncertain significance	6	3259116	3259116	Human		name
156073171	CV2240657	single nucleotide variant	NM_001128591.2(PSMG4):c.197C>T (p.Ser66Phe)	not specified [RCV004119291]	uncertain significance	6	3263706	3263706	Human		name
405672149	CV3378656	single nucleotide variant	NM_001128591.2(PSMG4):c.101C>T (p.Thr34Met)	not specified [RCV004515408]	uncertain significance	6	3259123	3259123	Human		name
407531805	CV3471963	single nucleotide variant	NM_001128591.2(PSMG4):c.121G>C (p.Val41Leu)	not specified [RCV004657793]	uncertain significance	6	3259143	3259143	Human		name
597750437	CV3592176	single nucleotide variant	NM_001128591.2(PSMG4):c.253A>G (p.Arg85Gly)	not specified [RCV004846459]	uncertain significance	6	3267593	3267593	Human		name
597750447	CV3592178	single nucleotide variant	NM_001128591.2(PSMG4):c.289C>T (p.Leu97Phe)	not specified [RCV004846461]	uncertain significance	6	3267629	3267629	Human		name
597750460	CV3592181	single nucleotide variant	NM_001128591.2(PSMG4):c.152C>T (p.Ala51Val)	not specified [RCV004846464]	uncertain significance	6	3259174	3259174	Human		name
329352421	CV2453000	single nucleotide variant	NM_001128591.2(PSMG4):c.313G>A (p.Ala105Thr)	not specified [RCV004277623]	uncertain significance	6	3267653	3267653	Human		name
597750442	CV3592177	single nucleotide variant	NM_001128591.2(PSMG4):c.347T>C (p.Met116Thr)	not specified [RCV004846460]	uncertain significance	6	3267687	3267687	Human		name