Dclk1 Variant Search Result - Rat Genome Database

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25 records found for search term Dclk1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582799	CV117355	single nucleotide variant	NM_004734.4(DCLK1):c.724-44500G>T	Lung cancer [RCV000097876]	uncertain significance	13	35991957	35991957	Human		name
8582800	CV117356	single nucleotide variant	NM_004734.4(DCLK1):c.723+48717C>T	Lung cancer [RCV000097877]	uncertain significance	13	36063152	36063152	Human		name
156341371	CV2225817	single nucleotide variant	NM_001330071.2(DCLK1):c.2058+5084G>C	not specified [RCV004103222]	uncertain significance	13	35788282	35788282	Human		name
329351639	CV2459217	single nucleotide variant	NM_001330071.2(DCLK1):c.95G>T (p.Ser32Ile)	not specified [RCV004274656]	uncertain significance	13	36126043	36126043	Human		name
405691061	CV3246754	single nucleotide variant	NM_001330071.2(DCLK1):c.65G>T (p.Ser22Ile)	not specified [RCV004373324]	uncertain significance	13	36126073	36126073	Human		name
598262277	CV3963690	single nucleotide variant	NM_001330071.2(DCLK1):c.46G>A (p.Asp16Asn)	not specified [RCV005325351]	uncertain significance	13	36126092	36126092	Human		name
8627441	CV82585	single nucleotide variant	NM_001195415.1(DCLK1):c.831C>T (p.Phe277=)	Malignant melanoma [RCV000062665]	not provided	13	35809032	35809032	Human		name
597800924	CV3652109	single nucleotide variant	NM_001330071.2(DCLK1):c.145A>T (p.Thr49Ser)	not specified [RCV004905967]	uncertain significance	13	36125993	36125993	Human		name
597800926	CV3652110	single nucleotide variant	NM_001330071.2(DCLK1):c.294C>G (p.Asn98Lys)	not specified [RCV004905968]	uncertain significance	13	36125844	36125844	Human		name
15164690	CV702680	single nucleotide variant	NM_001330071.2(DCLK1):c.1506G>A (p.Leu502=)	not provided [RCV000948407]	benign	13	35822777	35822777	Human		name
15180863	CV739040	single nucleotide variant	NM_001330071.2(DCLK1):c.1452C>T (p.Thr484=)	not provided [RCV000907455]	benign	13	35822831	35822831	Human		name
155915414	CV2200270	single nucleotide variant	NM_001330071.2(DCLK1):c.910C>T (p.Arg304Cys)	not specified [RCV004076611]	uncertain significance	13	35871254	35871254	Human		name
155989539	CV2352228	single nucleotide variant	NM_001330071.2(DCLK1):c.500C>T (p.Ala167Val)	not specified [RCV004200708]	uncertain significance	13	36112092	36112092	Human		name
405691055	CV3246753	single nucleotide variant	NM_001330071.2(DCLK1):c.460G>A (p.Val154Ile)	not specified [RCV004373323]	uncertain significance	13	36112132	36112132	Human		name
407458119	CV3430316	single nucleotide variant	NM_001330071.2(DCLK1):c.515G>A (p.Ser172Asn)	not specified [RCV004611417]	uncertain significance	13	36112077	36112077	Human		name
597800927	CV3652111	single nucleotide variant	NM_001330071.2(DCLK1):c.493T>C (p.Ser165Pro)	not specified [RCV004905969]	uncertain significance	13	36112099	36112099	Human		name
155997205	CV2373157	single nucleotide variant	NM_001330071.2(DCLK1):c.1462G>A (p.Ala488Thr)	not specified [RCV004217842]	uncertain significance	13	35822821	35822821	Human		name
155929502	CV2389175	single nucleotide variant	NM_001330071.2(DCLK1):c.1069G>A (p.Ala357Thr)	not specified [RCV004235502]	uncertain significance	13	35839143	35839143	Human		name
401901844	CV2813855	single nucleotide variant	NM_001330071.2(DCLK1):c.1852G>A (p.Asp618Asn)	not provided [RCV003393279]	uncertain significance	13	35808235	35808235	Human		name
405691040	CV3246750	single nucleotide variant	NM_001330071.2(DCLK1):c.1025G>A (p.Arg342Gln)	not specified [RCV004373320]	uncertain significance	13	35854509	35854509	Human		name
405691045	CV3246751	single nucleotide variant	NM_001330071.2(DCLK1):c.1687G>A (p.Gly563Arg)	not specified [RCV004373321]	uncertain significance	13	35810836	35810836	Human		name
405691049	CV3246752	single nucleotide variant	NM_001330071.2(DCLK1):c.1880T>C (p.Met627Thr)	not specified [RCV004373322]	uncertain significance	13	35805763	35805763	Human		name
407458117	CV3430315	single nucleotide variant	NM_001330071.2(DCLK1):c.2023C>T (p.Pro675Ser)	not specified [RCV004611416]	uncertain significance	13	35793401	35793401	Human		name
597800922	CV3652108	single nucleotide variant	NM_001330071.2(DCLK1):c.1780C>G (p.Gln594Glu)	not specified [RCV004905966]	uncertain significance	13	35808307	35808307	Human		name
597800929	CV3652112	single nucleotide variant	NM_001330071.2(DCLK1):c.1963A>T (p.Asn655Tyr)	not specified [RCV004905970]	uncertain significance	13	35793461	35793461	Human		name

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