Klk8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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26 records found for search term Klk8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156133864	CV2284615	single nucleotide variant	NM_007196.4(KLK8):c.71-87C>T	not specified [RCV004140778]	likely benign	19	51000670	51000670	Human		name
156247680	CV2357077	single nucleotide variant	NM_007196.4(KLK8):c.71-18C>G	not specified [RCV004206877]	uncertain significance	19	51000601	51000601	Human		name
405813987	CV3276442	single nucleotide variant	NM_007196.4(KLK8):c.71-132G>T	not specified [RCV004409678]	uncertain significance	19	51000715	51000715	Human		name
401891914	CV2775797	single nucleotide variant	NM_007196.4(KLK8):c.10C>A (p.Pro4Thr)	not specified [RCV004344842]	uncertain significance	19	51001158	51001158	Human		name
405814099	CV3276438	single nucleotide variant	NM_007196.4(KLK8):c.11C>A (p.Pro4His)	not specified [RCV004409674]	uncertain significance	19	51001157	51001157	Human		name
407499072	CV3448689	single nucleotide variant	NM_007196.4(KLK8):c.14G>A (p.Arg5Gln)	not specified [RCV004644219]	uncertain significance	19	51001154	51001154	Human		name
155979173	CV2340020	single nucleotide variant	NM_007196.4(KLK8):c.38T>C (p.Met13Thr)	not specified [RCV004192268]	uncertain significance	19	51001130	51001130	Human		name
407525082	CV3448692	single nucleotide variant	NM_007196.4(KLK8):c.55G>C (p.Gly19Arg)	not specified [RCV004631597]	uncertain significance	19	51001113	51001113	Human		name
597797216	CV3700923	single nucleotide variant	NM_007196.4(KLK8):c.630C>T (p.Gly210=)	not specified [RCV004935731]	likely benign	19	50996212	50996212	Human		name
598161961	CV3983857	single nucleotide variant	NM_007196.4(KLK8):c.642C>T (p.Gly214=)	not specified [RCV005368540]	likely benign	19	50996200	50996200	Human		name
156057575	CV2305160	single nucleotide variant	NM_007196.4(KLK8):c.143C>T (p.Ala48Val)	not specified [RCV004171102]	uncertain significance	19	51000511	51000511	Human		name
407499077	CV3448691	single nucleotide variant	NM_007196.4(KLK8):c.121C>T (p.Pro41Ser)	not specified [RCV004644220]	uncertain significance	19	51000533	51000533	Human		name
156063205	CV2240131	single nucleotide variant	NM_007196.4(KLK8):c.604A>G (p.Ser202Gly)	not specified [RCV004110895]	uncertain significance	19	50997774	50997774	Human		name
156193107	CV2301940	single nucleotide variant	NM_007196.4(KLK8):c.623G>A (p.Cys208Tyr)	not specified [RCV004156717]	uncertain significance	19	50997755	50997755	Human		name
401760107	CV2694925	single nucleotide variant	NM_007196.4(KLK8):c.730A>G (p.Asn244Asp)	not specified [RCV004301314]	uncertain significance	19	50996112	50996112	Human		name
401725471	CV2721789	single nucleotide variant	NM_007196.4(KLK8):c.331A>G (p.Ser111Gly)	not specified [RCV004326309]	uncertain significance	19	51000158	51000158	Human		name
405813981	CV3276439	single nucleotide variant	NM_007196.4(KLK8):c.451A>C (p.Lys151Gln)	not specified [RCV004409675]	uncertain significance	19	51000038	51000038	Human		name
405813983	CV3276440	single nucleotide variant	NM_007196.4(KLK8):c.553G>A (p.Glu185Lys)	not specified [RCV004409676]	uncertain significance	19	50997825	50997825	Human		name
405813989	CV3276443	single nucleotide variant	NM_007196.4(KLK8):c.709G>T (p.Asp237Tyr)	not specified [RCV004409679]	uncertain significance	19	50996133	50996133	Human		name
405813992	CV3276444	single nucleotide variant	NM_007196.4(KLK8):c.761A>C (p.Lys254Thr)	not specified [RCV004409680]	uncertain significance	19	50996081	50996081	Human		name
407499081	CV3448693	single nucleotide variant	NM_007196.4(KLK8):c.419G>A (p.Ser140Asn)	not specified [RCV004644221]	likely benign	19	51000070	51000070	Human		name
597797220	CV3700924	single nucleotide variant	NM_007196.4(KLK8):c.749A>C (p.Asp250Ala)	not specified [RCV004935732]	uncertain significance	19	50996093	50996093	Human		name
597797223	CV3700925	single nucleotide variant	NM_007196.4(KLK8):c.379C>T (p.Arg127Cys)	not specified [RCV004935733]	uncertain significance	19	51000110	51000110	Human		name
598161946	CV3983854	single nucleotide variant	NM_007196.4(KLK8):c.565C>T (p.Pro189Ser)	not specified [RCV005368537]	uncertain significance	19	50997813	50997813	Human		name
598161950	CV3983855	single nucleotide variant	NM_007196.4(KLK8):c.367C>G (p.Leu123Val)	not specified [RCV005368538]	uncertain significance	19	51000122	51000122	Human		name
598221519	CV3983858	single nucleotide variant	NM_007196.4(KLK8):c.475A>G (p.Thr159Ala)	not specified [RCV005360817]	uncertain significance	19	51000014	51000014	Human		name

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