Fam151b Variant Search Result - Rat Genome Database

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13 records found for search term Fam151b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598225058	CV3965921	single nucleotide variant	NM_205548.3(FAM151B):c.11C>G (p.Ser4Cys)	not specified [RCV005341384]	uncertain significance	5	80488134	80488134	Human		name
155918150	CV2195756	single nucleotide variant	NM_205548.3(FAM151B):c.77C>T (p.Thr26Ile)	not specified [RCV004076109]	uncertain significance	5	80501843	80501843	Human		name
155940211	CV2222028	single nucleotide variant	NM_205548.3(FAM151B):c.124A>G (p.Lys42Glu)	not specified [RCV004103014]	uncertain significance	5	80501890	80501890	Human		name
597737666	CV3668601	single nucleotide variant	NM_205548.3(FAM151B):c.217A>G (p.Ile73Val)	not specified [RCV004920885]	uncertain significance	5	80513669	80513669	Human		name
597737676	CV3668603	single nucleotide variant	NM_205548.3(FAM151B):c.277G>A (p.Val93Ile)	not specified [RCV004920887]	uncertain significance	5	80513729	80513729	Human		name
156083146	CV2244450	single nucleotide variant	NM_205548.3(FAM151B):c.573A>G (p.Ile191Met)	not specified [RCV004100415]	uncertain significance	5	80522040	80522040	Human		name
401872652	CV2793135	single nucleotide variant	NM_205548.3(FAM151B):c.463A>T (p.Ile155Leu)	not specified [RCV004360447]	uncertain significance	5	80519838	80519838	Human		name
405727342	CV3259899	single nucleotide variant	NM_205548.3(FAM151B):c.715G>A (p.Val239Ile)	not specified [RCV004378780]	likely benign	5	80541716	80541716	Human		name
407508112	CV3435510	single nucleotide variant	NM_205548.3(FAM151B):c.460G>A (p.Val154Met)	not specified [RCV004625315]	uncertain significance	5	80519835	80519835	Human		name
597737671	CV3668602	single nucleotide variant	NM_205548.3(FAM151B):c.809T>A (p.Ile270Asn)	not specified [RCV004920886]	uncertain significance	5	80541810	80541810	Human		name
597737683	CV3668604	single nucleotide variant	NM_205548.3(FAM151B):c.572T>C (p.Ile191Thr)	not specified [RCV004920888]	uncertain significance	5	80522039	80522039	Human		name
597737688	CV3668605	single nucleotide variant	NM_205548.3(FAM151B):c.315A>T (p.Lys105Asn)	not specified [RCV004920889]	uncertain significance	5	80513767	80513767	Human		name
598225054	CV3965920	single nucleotide variant	NM_205548.3(FAM151B):c.412C>G (p.Pro138Ala)	not specified [RCV005341383]	uncertain significance	5	80519787	80519787	Human		name