Fosb Variant Search Result - Rat Genome Database

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28 records found for search term Fosb

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598215919	CV3973672	single nucleotide variant	NM_006732.3(FOSB):c.92C>T (p.Ser31Phe)	not specified [RCV005339788]	uncertain significance	19	45468678	45468678	Human		name
15148322	CV716524	single nucleotide variant	NM_006732.3(FOSB):c.97G>A (p.Gly33Ser)	not provided [RCV000967521]	benign	19	45468683	45468683	Human		name
15200264	CV772749	single nucleotide variant	NM_006732.3(FOSB):c.537G>C (p.Leu179=)	not provided [RCV000935334]	likely benign	19	45471283	45471283	Human		name
15121595	CV772750	single nucleotide variant	NM_006732.3(FOSB):c.660G>A (p.Pro220=)	not provided [RCV000940551]	likely benign	19	45472655	45472655	Human		name
156279922	CV2224037	single nucleotide variant	NM_006732.3(FOSB):c.284A>C (p.Asp95Ala)	not specified [RCV004095912]	uncertain significance	19	45470786	45470786	Human		name
329385798	CV2432223	single nucleotide variant	NM_006732.3(FOSB):c.136G>T (p.Gly46Cys)	not specified [RCV004251153]	uncertain significance	19	45470638	45470638	Human		name
401723885	CV2725073	single nucleotide variant	NM_006732.3(FOSB):c.220A>G (p.Thr74Ala)	not specified [RCV004319824]	uncertain significance	19	45470722	45470722	Human		name
597725376	CV3672965	single nucleotide variant	NM_006732.3(FOSB):c.154G>A (p.Gly52Ser)	not specified [RCV004919200]	uncertain significance	19	45470656	45470656	Human		name
156245218	CV2218956	single nucleotide variant	NM_006732.3(FOSB):c.416G>A (p.Arg139Gln)	not specified [RCV004087138]	uncertain significance	19	45470918	45470918	Human		name
155900967	CV2241880	single nucleotide variant	NM_006732.3(FOSB):c.371C>T (p.Ser124Phe)	not specified [RCV004106799]	uncertain significance	19	45470873	45470873	Human		name
155982638	CV2244224	single nucleotide variant	NM_006732.3(FOSB):c.376A>G (p.Ser126Gly)	not specified [RCV004110712]	uncertain significance	19	45470878	45470878	Human		name
156136936	CV2280549	single nucleotide variant	NM_006732.3(FOSB):c.541G>A (p.Asp181Asn)	not specified [RCV004143036]	uncertain significance	19	45471287	45471287	Human		name
156261784	CV2282428	single nucleotide variant	NM_006732.3(FOSB):c.415C>G (p.Arg139Gly)	not specified [RCV004133239]	uncertain significance	19	45470917	45470917	Human		name
156245846	CV2283457	single nucleotide variant	NM_006732.3(FOSB):c.818C>G (p.Pro273Arg)	not specified [RCV004139677]	uncertain significance	19	45472813	45472813	Human		name
155954656	CV2302200	single nucleotide variant	NM_006732.3(FOSB):c.394C>T (p.Pro132Ser)	not specified [RCV004159200]	uncertain significance	19	45470896	45470896	Human		name
156076768	CV2331832	single nucleotide variant	NM_006732.3(FOSB):c.709G>A (p.Glu237Lys)	not specified [RCV004184446]	uncertain significance	19	45472704	45472704	Human		name
156232320	CV2346102	single nucleotide variant	NM_006732.3(FOSB):c.390T>G (p.Ser130Arg)	not specified [RCV004201566]	uncertain significance	19	45470892	45470892	Human		name
156306946	CV2369562	single nucleotide variant	NM_006732.3(FOSB):c.805A>G (p.Ser269Gly)	not specified [RCV004214981]	uncertain significance	19	45472800	45472800	Human		name
401765635	CV2683370	single nucleotide variant	NM_006732.3(FOSB):c.759C>A (p.Ser253Arg)	not specified [RCV004288142]	uncertain significance	19	45472754	45472754	Human		name
401759558	CV2690940	single nucleotide variant	NM_006732.3(FOSB):c.340A>C (p.Ser114Arg)	not specified [RCV004298625]	uncertain significance	19	45470842	45470842	Human		name
405746496	CV3253829	single nucleotide variant	NM_006732.3(FOSB):c.379G>A (p.Gly127Arg)	not specified [RCV004392093]	uncertain significance	19	45470881	45470881	Human		name
405746504	CV3253830	single nucleotide variant	NM_006732.3(FOSB):c.541G>C (p.Asp181His)	not specified [RCV004392094]	uncertain significance	19	45471287	45471287	Human		name
405746514	CV3253831	single nucleotide variant	NM_006732.3(FOSB):c.670A>T (p.Ile224Phe)	not specified [RCV004392095]	uncertain significance	19	45472665	45472665	Human		name
407510384	CV3432574	single nucleotide variant	NM_006732.3(FOSB):c.820C>T (p.Pro274Ser)	not specified [RCV004626094]	uncertain significance	19	45472815	45472815	Human		name
407510387	CV3432575	single nucleotide variant	NM_006732.3(FOSB):c.937G>A (p.Ala313Thr)	not specified [RCV004626095]	uncertain significance	19	45472932	45472932	Human		name
597725361	CV3672962	single nucleotide variant	NM_006732.3(FOSB):c.446C>T (p.Thr149Met)	not specified [RCV004919198]	uncertain significance	19	45470948	45470948	Human		name
597725368	CV3672964	single nucleotide variant	NM_006732.3(FOSB):c.433C>T (p.Pro145Ser)	not specified [RCV004919199]	uncertain significance	19	45470935	45470935	Human		name
598215926	CV3973673	single nucleotide variant	NM_006732.3(FOSB):c.1009G>A (p.Ala337Thr)	not specified [RCV005339789]	uncertain significance	19	45473004	45473004	Human		name

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