Klk11 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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35 records found for search term Klk11

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329387631	CV2446736	single nucleotide variant	NM_001136032.3(KLK11):c.-11C>T	Inborn genetic diseases [RCV003190230]	uncertain significance	19	51025642	51025642	Human	1	name
401877057	CV2793332	single nucleotide variant	NM_001136032.3(KLK11):c.-21C>G	Inborn genetic diseases [RCV003383624]	uncertain significance	19	51025652	51025652	Human	1	name
405813890	CV3276371	single nucleotide variant	NM_001136032.3(KLK11):c.-11C>G	Inborn genetic diseases [RCV004409607]	uncertain significance	19	51025642	51025642	Human	1	name
596946966	CV3547026	single nucleotide variant	NM_001136032.3(KLK11):c.-10C>G	not provided [RCV004810832]	likely benign	19	51025641	51025641	Human		name
156396153	CV2326123	single nucleotide variant	NM_144947.3(KLK11):c.25G>T (p.Asp9Tyr)	Inborn genetic diseases [RCV002944836]	uncertain significance	19	51027493	51027493	Human	1	name
598161868	CV3983822	single nucleotide variant	NM_144947.3(KLK11):c.22C>T (p.Arg8Trp)	Inborn genetic diseases [RCV005368521]	uncertain significance	19	51027496	51027496	Human	1	name
155915626	CV2239513	single nucleotide variant	NM_144947.3(KLK11):c.52A>G (p.Thr18Ala)	Inborn genetic diseases [RCV002772243]	likely benign	19	51027466	51027466	Human	1	name
405813884	CV3276368	single nucleotide variant	NM_144947.3(KLK11):c.41G>A (p.Gly14Asp)	Inborn genetic diseases [RCV004409604]	likely benign	19	51027477	51027477	Human	1	name
8636951	CV92176	single nucleotide variant	NM_144947.1(KLK11):c.83C>T (p.Ser28Phe)	Malignant melanoma [RCV000072274]	not provided	19	51025645	51025645	Human		name
156138874	CV2250337	single nucleotide variant	NM_001136032.3(KLK11):c.79G>A (p.Glu27Lys)	Inborn genetic diseases [RCV002826060]	uncertain significance	19	51024756	51024756	Human	1	name
401829889	CV2744758	single nucleotide variant	NM_001136032.3(KLK11):c.53G>A (p.Gly18Glu)	Ichthyosis with erythrokeratoderma [RCV003328132]\|not provided [RCV004721177]	pathogenic	19	51024782	51024782	Human	1	name
401829890	CV2744759	single nucleotide variant	NM_001136032.3(KLK11):c.52G>A (p.Gly18Arg)	Ichthyosis with erythrokeratoderma [RCV003328133]	pathogenic	19	51024783	51024783	Human	1	name
155924592	CV2352108	single nucleotide variant	NM_001136032.3(KLK11):c.296A>G (p.Asn99Ser)	Inborn genetic diseases [RCV002969865]	uncertain significance	19	51024212	51024212	Human	1	name
156103308	CV2363359	single nucleotide variant	NM_001136032.3(KLK11):c.200G>A (p.Arg67His)	Inborn genetic diseases [RCV002662116]	uncertain significance	19	51024308	51024308	Human	1	name
401864823	CV2757212	single nucleotide variant	NM_001136032.3(KLK11):c.289G>A (p.Gly97Ser)	Inborn genetic diseases [RCV003344433]	uncertain significance	19	51024219	51024219	Human	1	name
405813881	CV3276367	single nucleotide variant	NM_001136032.3(KLK11):c.146C>T (p.Ala49Val)	Inborn genetic diseases [RCV004409603]	uncertain significance	19	51024689	51024689	Human	1	name
407525070	CV3448665	single nucleotide variant	NM_001136032.3(KLK11):c.292T>C (p.Phe98Leu)	Inborn genetic diseases [RCV004631591]	uncertain significance	19	51024216	51024216	Human	1	name
597686064	CV3700872	single nucleotide variant	NM_001136032.3(KLK11):c.244G>T (p.Gly82Cys)	Inborn genetic diseases [RCV004984088]	uncertain significance	19	51024264	51024264	Human	1	name
597686089	CV3700876	single nucleotide variant	NM_001136032.3(KLK11):c.257C>A (p.Thr86Asn)	Inborn genetic diseases [RCV004984091]	uncertain significance	19	51024251	51024251	Human	1	name
597686095	CV3700877	single nucleotide variant	NM_001136032.3(KLK11):c.272A>T (p.Glu91Val)	Inborn genetic diseases [RCV004984092]	uncertain significance	19	51024236	51024236	Human	1	name
598161871	CV3983824	single nucleotide variant	NM_001136032.3(KLK11):c.245G>C (p.Gly82Ala)	Inborn genetic diseases [RCV005368522]	uncertain significance	19	51024263	51024263	Human	1	name
155924173	CV2280482	single nucleotide variant	NM_001136032.3(KLK11):c.479C>T (p.Thr160Ile)	Inborn genetic diseases [RCV002860081]	uncertain significance	19	51023213	51023213	Human	1	name
156047575	CV2319176	single nucleotide variant	NM_001136032.3(KLK11):c.483G>C (p.Leu161Phe)	Inborn genetic diseases [RCV002949920]	uncertain significance	19	51023209	51023209	Human	1	name
156334255	CV2333360	single nucleotide variant	NM_001136032.3(KLK11):c.737C>T (p.Thr246Met)	Inborn genetic diseases [RCV002964540]	uncertain significance	19	51022561	51022561	Human	1	name
329387037	CV2436225	single nucleotide variant	NM_001136032.3(KLK11):c.701C>T (p.Thr234Met)	Inborn genetic diseases [RCV003189924]	uncertain significance	19	51022597	51022597	Human	1	name
401742166	CV2676909	single nucleotide variant	NM_001136032.3(KLK11):c.326A>G (p.Asn109Ser)	Inborn genetic diseases [RCV003251622]	uncertain significance	19	51024182	51024182	Human	1	name
405813886	CV3276369	single nucleotide variant	NM_001136032.3(KLK11):c.352T>A (p.Ser118Thr)	Inborn genetic diseases [RCV004409605]	likely benign	19	51024156	51024156	Human	1	name
405813888	CV3276370	single nucleotide variant	NM_001136032.3(KLK11):c.380G>A (p.Arg127Gln)	Inborn genetic diseases [RCV004409606]	uncertain significance	19	51024128	51024128	Human	1	name
597686073	CV3700873	single nucleotide variant	NM_001136032.3(KLK11):c.401G>T (p.Arg134Leu)	Inborn genetic diseases [RCV004984089]	uncertain significance	19	51024107	51024107	Human	1	name
597686082	CV3700875	single nucleotide variant	NM_001136032.3(KLK11):c.496A>G (p.Ile166Val)	Inborn genetic diseases [RCV004984090]	uncertain significance	19	51023196	51023196	Human	1	name
597686102	CV3700878	single nucleotide variant	NM_001136032.3(KLK11):c.449C>T (p.Thr150Met)	Inborn genetic diseases [RCV004984093]	uncertain significance	19	51024059	51024059	Human	1	name
597686108	CV3700879	single nucleotide variant	NM_001136032.3(KLK11):c.574C>G (p.Gln192Glu)	Inborn genetic diseases [RCV004984094]	uncertain significance	19	51023118	51023118	Human	1	name
598161865	CV3983820	single nucleotide variant	NM_001136032.3(KLK11):c.466C>A (p.Arg156Ser)	Inborn genetic diseases [RCV005368520]	uncertain significance	19	51023226	51023226	Human	1	name
598221472	CV3983821	single nucleotide variant	NM_001136032.3(KLK11):c.323G>A (p.Arg108His)	Inborn genetic diseases [RCV005360810]	uncertain significance	19	51024185	51024185	Human	1	name
598183121	CV3983823	single nucleotide variant	NM_001136032.3(KLK11):c.322C>T (p.Arg108Cys)	Inborn genetic diseases [RCV005352845]	uncertain significance	19	51024186	51024186	Human	1	name

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