Nkx2-2 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

44 records found for search term Nkx2-2

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150470452	CV1269847	single nucleotide variant	NM_002509.4(NKX2-2):c.-75G>A	not provided [RCV001695134]	benign	20	21513744	21513744	Human		name
156202364	CV1925728	single nucleotide variant	NM_002509.4(NKX2-2):c.260-4C>G	not provided [RCV002643678]	likely benign	20	21512489	21512489	Human		name
156411681	CV1972574	single nucleotide variant	NM_002509.4(NKX2-2):c.260-4C>T	not provided [RCV002587571]	likely benign	20	21512489	21512489	Human		name
150449105	CV1260778	single nucleotide variant	NM_002509.4(NKX2-2):c.259+274G>T	not provided [RCV001680447]	benign	20	21513137	21513137	Human		name
152076821	CV1564573	single nucleotide variant	NM_002509.4(NKX2-2):c.6G>T (p.Ser2=)	not provided [RCV002192519]	likely benign	20	21513664	21513664	Human		name
151355941	CV1327124	single nucleotide variant	NM_002509.4(NKX2-2):c.33G>T (p.Ser11=)	not provided [RCV003542348]\|not specified [RCV001822294]	likely benign	20	21513637	21513637	Human		name
597956043	CV3754526	single nucleotide variant	NM_002509.4(NKX2-2):c.96G>A (p.Pro32=)	not provided [RCV005080376]	likely benign	20	21513574	21513574	Human		name
155970529	CV1888958	single nucleotide variant	NM_002509.4(NKX2-2):c.259C>T (p.Leu87=)	NKX2-2-related disorder [RCV003963592]\|not provided [RCV003075155]	likely benign\|uncertain significance	20	21513411	21513411	Human		name , trait , alternate_id
156055178	CV2003271	single nucleotide variant	NM_002509.4(NKX2-2):c.192C>T (p.Pro64=)	not provided [RCV002659496]	likely benign	20	21513478	21513478	Human		name
405200446	CV2877176	single nucleotide variant	NM_002509.4(NKX2-2):c.135C>T (p.Ala45=)	not provided [RCV003551333]	likely benign	20	21513535	21513535	Human		name
405259293	CV3194703	single nucleotide variant	NM_002509.4(NKX2-2):c.267T>C (p.Gly89=)	NKX2-2-related disorder [RCV003894095]	likely benign	20	21512478	21512478	Human		name , trait , alternate_id
597898104	CV3740786	single nucleotide variant	NM_002509.4(NKX2-2):c.153C>A (p.Gly51=)	not provided [RCV005071949]	likely benign	20	21513517	21513517	Human		name
597923324	CV3839968	single nucleotide variant	NM_002509.4(NKX2-2):c.108C>T (p.Asn36=)	not provided [RCV005184707]	likely benign	20	21513562	21513562	Human		name
127314471	CV1158758	single nucleotide variant	NM_002509.4(NKX2-2):c.95C>T (p.Pro32Leu)	not provided [RCV001519639]\|not specified [RCV001821832]	benign	20	21513575	21513575	Human		name
152141283	CV1628915	single nucleotide variant	NM_002509.4(NKX2-2):c.723G>A (p.Ser241=)	not provided [RCV002100811]	likely benign	20	21512022	21512022	Human		name
156413833	CV1905583	single nucleotide variant	NM_002509.4(NKX2-2):c.94C>G (p.Pro32Ala)	not provided [RCV003073464]	uncertain significance	20	21513576	21513576	Human		name
156013813	CV1912597	single nucleotide variant	NM_002509.4(NKX2-2):c.369G>A (p.Gly123=)	not provided [RCV002619040]	likely benign	20	21512376	21512376	Human		name
156126830	CV1930668	single nucleotide variant	NM_002509.4(NKX2-2):c.717G>T (p.Ala239=)	not provided [RCV002640549]	likely benign	20	21512028	21512028	Human		name
405211365	CV2868041	single nucleotide variant	NM_002509.4(NKX2-2):c.534C>T (p.Asn178=)	not provided [RCV003552646]	likely benign	20	21512211	21512211	Human		name
405227040	CV3069465	single nucleotide variant	NM_002509.4(NKX2-2):c.606G>T (p.Arg202=)	not provided [RCV003734231]	benign	20	21512139	21512139	Human		name
405165285	CV3125580	single nucleotide variant	NM_002509.4(NKX2-2):c.385C>A (p.Arg129=)	not provided [RCV003818663]	likely benign	20	21512360	21512360	Human		name
405086869	CV3133988	single nucleotide variant	NM_002509.4(NKX2-2):c.462G>T (p.Ser154=)	not provided [RCV003834526]	likely benign	20	21512283	21512283	Human		name
402495693	CV3179160	single nucleotide variant	NM_002509.4(NKX2-2):c.693C>A (p.Gly231=)	not provided [RCV003877427]	likely benign	20	21512052	21512052	Human		name
597969824	CV3791722	single nucleotide variant	NM_002509.4(NKX2-2):c.459G>T (p.Leu153=)	not provided [RCV005141539]	likely benign	20	21512286	21512286	Human		name
597848841	CV3793015	single nucleotide variant	NM_002509.4(NKX2-2):c.708C>A (p.Ala236=)	not provided [RCV005145151]	likely benign	20	21512037	21512037	Human		name
597971943	CV3833257	single nucleotide variant	NM_002509.4(NKX2-2):c.363C>G (p.Gly121=)	not provided [RCV005167154]	likely benign	20	21512382	21512382	Human		name
597926223	CV3840660	single nucleotide variant	NM_002509.4(NKX2-2):c.588C>G (p.Pro196=)	not provided [RCV005185131]	likely benign	20	21512157	21512157	Human		name
150442997	CV1264527	single nucleotide variant	NM_002509.4(NKX2-2):c.124G>A (p.Ala42Thr)	not provided [RCV001679511]	benign	20	21513546	21513546	Human		name
151353637	CV1327189	single nucleotide variant	NM_002509.4(NKX2-2):c.108C>A (p.Asn36Lys)	not provided [RCV002542513]\|not specified [RCV001817133]	benign\|likely benign	20	21513562	21513562	Human		name
151354712	CV1327779	single nucleotide variant	NM_002509.4(NKX2-2):c.296C>T (p.Ser99Leu)	not specified [RCV001819254]	uncertain significance	20	21512449	21512449	Human		name
151770006	CV1504145	single nucleotide variant	NM_002509.4(NKX2-2):c.286C>A (p.Pro96Thr)	not provided [RCV002045154]	uncertain significance	20	21512459	21512459	Human		name
156226689	CV2216028	single nucleotide variant	NM_002509.4(NKX2-2):c.223C>A (p.Arg75Ser)	Inborn genetic diseases [RCV002712487]	uncertain significance	20	21513447	21513447	Human	1	name
156382426	CV2227355	single nucleotide variant	NM_002509.4(NKX2-2):c.266G>A (p.Gly89Asp)	Inborn genetic diseases [RCV002722776]	uncertain significance	20	21512479	21512479	Human	1	name
405132225	CV2905525	deletion	NM_002509.4(NKX2-2):c.356del (p.Pro119fs)	not provided [RCV003560136]	likely pathogenic	20	21512389	21512389	Human		name
405277984	CV3205262	single nucleotide variant	NM_002509.4(NKX2-2):c.121C>T (p.Pro41Ser)	NKX2-2-related disorder [RCV003954304]\|not provided [RCV005102934]	likely benign	20	21513549	21513549	Human		name , trait , alternate_id
408366203	CV3516801	single nucleotide variant	NM_002509.4(NKX2-2):c.206G>A (p.Ser69Asn)	NKX2-2-related disorder [RCV004755684]	uncertain significance	20	21513464	21513464	Human		name , trait , alternate_id
151808889	CV1362840	single nucleotide variant	NM_002509.4(NKX2-2):c.716C>T (p.Ala239Val)	not provided [RCV001991631]	uncertain significance	20	21512029	21512029	Human		name
151819222	CV1463111	single nucleotide variant	NM_002509.4(NKX2-2):c.730C>T (p.His244Tyr)	not provided [RCV002049622]	uncertain significance	20	21512015	21512015	Human		name
152142656	CV1654392	single nucleotide variant	NM_002509.4(NKX2-2):c.365G>C (p.Gly122Ala)	not provided [RCV002200776]	benign	20	21512380	21512380	Human		name
401907598	CV2801165	single nucleotide variant	NM_002509.4(NKX2-2):c.524G>A (p.Trp175Ter)	NKX2-2-related disorder [RCV003397406]	uncertain significance	20	21512221	21512221	Human		name , trait , alternate_id
405236099	CV2887841	single nucleotide variant	NM_002509.4(NKX2-2):c.677C>T (p.Ala226Val)	not provided [RCV003556418]	likely benign	20	21512068	21512068	Human		name
405706845	CV3362261	single nucleotide variant	NM_002509.4(NKX2-2):c.688G>A (p.Ala230Thr)	Inborn genetic diseases [RCV004493249]	uncertain significance	20	21512057	21512057	Human	1	name
405706853	CV3362262	single nucleotide variant	NM_002509.4(NKX2-2):c.781A>G (p.Thr261Ala)	Inborn genetic diseases [RCV004493250]	uncertain significance	20	21511964	21511964	Human	1	name
8628471	CV83615	single nucleotide variant	NM_002509.3(NKX2-2):c.704C>T (p.Ser235Phe)	Malignant melanoma [RCV000063696]	not provided	20	21512041	21512041	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message