Psmb6 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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22 records found for search term Psmb6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156308520	CV2369937	single nucleotide variant	NM_002798.3(PSMB6):c.25C>T (p.Arg9Trp)	not specified [RCV004208402]	uncertain significance	17	4796219	4796219	Human		name
598170704	CV3908129	single nucleotide variant	NM_002798.3(PSMB6):c.88G>A (p.Glu30Lys)	not specified [RCV005263169]	uncertain significance	17	4796282	4796282	Human		name
155917043	CV2278517	single nucleotide variant	NM_002798.3(PSMB6):c.221G>A (p.Arg74His)	not specified [RCV004132954]	likely benign	17	4797488	4797488	Human		name
401721920	CV2680741	single nucleotide variant	NM_002798.3(PSMB6):c.130G>T (p.Gly44Trp)	not specified [RCV004291350]	uncertain significance	17	4796755	4796755	Human		name
401721595	CV2710051	single nucleotide variant	NM_002798.3(PSMB6):c.112A>G (p.Met38Val)	not specified [RCV004315112]	uncertain significance	17	4796737	4796737	Human		name
405661950	CV3378523	single nucleotide variant	NM_002798.3(PSMB6):c.106A>G (p.Thr36Ala)	not specified [RCV004513297]	uncertain significance	17	4796731	4796731	Human		name
405661953	CV3378524	single nucleotide variant	NM_002798.3(PSMB6):c.209C>G (p.Pro70Arg)	not specified [RCV004513298]	uncertain significance	17	4797476	4797476	Human		name
598170701	CV3908128	single nucleotide variant	NM_002798.3(PSMB6):c.116C>T (p.Ala39Val)	not specified [RCV005263168]	uncertain significance	17	4796741	4796741	Human		name
156002411	CV2288019	single nucleotide variant	NM_002798.3(PSMB6):c.562C>A (p.Gln188Lys)	not specified [RCV004147780]	uncertain significance	17	4798138	4798138	Human		name
155906839	CV2357393	single nucleotide variant	NM_002798.3(PSMB6):c.481A>G (p.Ile161Val)	not specified [RCV004200275]	uncertain significance	17	4798057	4798057	Human		name
156102637	CV2386855	single nucleotide variant	NM_002798.3(PSMB6):c.701C>A (p.Ala234Asp)	not specified [RCV004233493]	uncertain significance	17	4798403	4798403	Human		name
329361288	CV2459423	single nucleotide variant	NM_002798.3(PSMB6):c.452G>A (p.Gly151Glu)	not specified [RCV004275113]	uncertain significance	17	4798028	4798028	Human		name
401876499	CV2767612	single nucleotide variant	NM_002798.3(PSMB6):c.697G>A (p.Val233Ile)	not specified [RCV004343756]	likely benign	17	4798399	4798399	Human		name
405661957	CV3378525	single nucleotide variant	NM_002798.3(PSMB6):c.694G>A (p.Ala232Thr)	not specified [RCV004513299]	likely benign	17	4798396	4798396	Human		name
407531691	CV3471881	single nucleotide variant	NM_002798.3(PSMB6):c.500C>T (p.Ser167Phe)	not specified [RCV004657735]	uncertain significance	17	4798076	4798076	Human		name
597749874	CV3592019	single nucleotide variant	NM_002798.3(PSMB6):c.425G>C (p.Gly142Ala)	not specified [RCV004846314]	uncertain significance	17	4797804	4797804	Human		name
597749879	CV3592020	single nucleotide variant	NM_002798.3(PSMB6):c.450G>C (p.Met150Ile)	not specified [RCV004846315]	uncertain significance	17	4798026	4798026	Human		name
597749883	CV3592021	single nucleotide variant	NM_002798.3(PSMB6):c.463G>A (p.Val155Ile)	not specified [RCV004846316]	uncertain significance	17	4798039	4798039	Human		name
597749890	CV3592022	single nucleotide variant	NM_002798.3(PSMB6):c.533G>A (p.Arg178Gln)	not specified [RCV004846317]	uncertain significance	17	4798109	4798109	Human		name
598170688	CV3908124	single nucleotide variant	NM_002798.3(PSMB6):c.548A>G (p.Lys183Arg)	not specified [RCV005263165]	uncertain significance	17	4798124	4798124	Human		name
598170693	CV3908126	single nucleotide variant	NM_002798.3(PSMB6):c.403G>C (p.Ala135Pro)	not specified [RCV005263166]	uncertain significance	17	4797782	4797782	Human		name
598170696	CV3908127	single nucleotide variant	NM_002798.3(PSMB6):c.638T>G (p.Ile213Ser)	not specified [RCV005263167]	uncertain significance	17	4798340	4798340	Human		name

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