Gk5 Variant Search Result - Rat Genome Database

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22 records found for search term Gk5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405867617	CV2842342	single nucleotide variant	NM_001039547.3(GK5):c.318-5T>C	EBV-positive nodal T- and NK-cell lymphoma [RCV004560291]	likely benign	3	142204793	142204793	Human		name
597707408	CV3681160	single nucleotide variant	NM_001039547.3(GK5):c.8G>A (p.Gly3Glu)	not specified [RCV004917091]	uncertain significance	3	142225448	142225448	Human		name
156352771	CV2324044	single nucleotide variant	NM_001039547.3(GK5):c.22C>T (p.Pro8Ser)	not specified [RCV004178344]	uncertain significance	3	142225434	142225434	Human		name
401893439	CV2763411	single nucleotide variant	NM_001039547.3(GK5):c.179T>A (p.Val60Glu)	not specified [RCV004349300]	uncertain significance	3	142215661	142215661	Human		name
405752355	CV3251584	single nucleotide variant	NM_001039547.3(GK5):c.220G>A (p.Val74Ile)	not specified [RCV004392931]	uncertain significance	3	142215620	142215620	Human		name
407519553	CV3443295	single nucleotide variant	NM_001039547.3(GK5):c.116C>A (p.Ala39Glu)	not specified [RCV004629635]	uncertain significance	3	142225340	142225340	Human		name
597759606	CV3681162	single nucleotide variant	NM_001039547.3(GK5):c.127T>C (p.Cys43Arg)	not specified [RCV004925540]	likely benign	3	142225329	142225329	Human		name
156130151	CV2209953	single nucleotide variant	NM_001039547.3(GK5):c.976C>G (p.Gln326Glu)	not specified [RCV004076398]	uncertain significance	3	142181533	142181533	Human		name
156255582	CV2219675	single nucleotide variant	NM_001039547.3(GK5):c.593C>G (p.Thr198Ser)	not specified [RCV004095392]	uncertain significance	3	142187730	142187730	Human		name
156068450	CV2237052	single nucleotide variant	NM_001039547.3(GK5):c.907A>G (p.Ile303Val)	not specified [RCV004113028]	likely benign	3	142182959	142182959	Human		name
405752361	CV3251585	single nucleotide variant	NM_001039547.3(GK5):c.518T>C (p.Val173Ala)	not specified [RCV004392932]	likely benign	3	142198827	142198827	Human		name
405752368	CV3251586	single nucleotide variant	NM_001039547.3(GK5):c.679A>G (p.Lys227Glu)	not specified [RCV004392933]	likely benign	3	142186454	142186454	Human		name
598251979	CV3977758	single nucleotide variant	NM_001039547.3(GK5):c.596G>T (p.Trp199Leu)	not specified [RCV005346008]	uncertain significance	3	142187727	142187727	Human		name
598220667	CV3977759	single nucleotide variant	NM_001039547.3(GK5):c.597G>T (p.Trp199Cys)	not specified [RCV005340487]	uncertain significance	3	142187726	142187726	Human		name
598251985	CV3977760	single nucleotide variant	NM_001039547.3(GK5):c.974G>A (p.Gly325Glu)	not specified [RCV005346009]	uncertain significance	3	142181535	142181535	Human		name
598251990	CV3977762	single nucleotide variant	NM_001039547.3(GK5):c.925C>T (p.Leu309Phe)	not specified [RCV005346010]	uncertain significance	3	142182941	142182941	Human		name
156146231	CV2357922	single nucleotide variant	NM_001039547.3(GK5):c.1001G>C (p.Ser334Thr)	not specified [RCV004209708]	uncertain significance	3	142181508	142181508	Human		name
401863819	CV2770846	single nucleotide variant	NM_001039547.3(GK5):c.1561C>T (p.Arg521Cys)	not specified [RCV004349876]	uncertain significance	3	142165651	142165651	Human		name
405752345	CV3251583	single nucleotide variant	NM_001039547.3(GK5):c.1513T>C (p.Cys505Arg)	not specified [RCV004392930]	uncertain significance	3	142165699	142165699	Human		name
597759596	CV3681159	single nucleotide variant	NM_001039547.3(GK5):c.1532G>A (p.Ser511Asn)	not specified [RCV004925538]	likely benign	3	142165680	142165680	Human		name
597759601	CV3681161	single nucleotide variant	NM_001039547.3(GK5):c.1350G>A (p.Met450Ile)	not specified [RCV004925539]	uncertain significance	3	142170416	142170416	Human		name
598220676	CV3977761	single nucleotide variant	NM_001039547.3(GK5):c.1484G>T (p.Ser495Ile)	not specified [RCV005340488]	uncertain significance	3	142165728	142165728	Human		name

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