Gas2l1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

32 records found for search term Gas2l1

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8637608	CV92834	single nucleotide variant	NM_152236.2(GAS2L1):c.246C>T (p.Ala82=)	Malignant melanoma [RCV000072932]	not provided	22	29308351	29308351	Human		name
8637609	CV92835	single nucleotide variant	NM_152236.2(GAS2L1):c.678C>T (p.Pro226=)	Malignant melanoma [RCV000072933]	not provided	22	29310483	29310483	Human		name
597754699	CV3680997	single nucleotide variant	NM_001362985.3(GAS2L1):c.19G>A (p.Gly7Ser)	not specified [RCV004924436]	uncertain significance	22	29308124	29308124	Human		name
156344894	CV2381980	single nucleotide variant	NM_001362985.3(GAS2L1):c.41A>G (p.Lys14Arg)	not specified [RCV004225910]	uncertain significance	22	29308146	29308146	Human		name
405765327	CV3251462	single nucleotide variant	NM_001362985.3(GAS2L1):c.58C>A (p.Arg20Ser)	not specified [RCV004394979]	uncertain significance	22	29308163	29308163	Human		name
598204450	CV3974135	single nucleotide variant	NM_001362985.3(GAS2L1):c.59G>A (p.Arg20His)	not specified [RCV005337427]	uncertain significance	22	29308164	29308164	Human		name
156067815	CV2221943	single nucleotide variant	NM_001362985.3(GAS2L1):c.164G>C (p.Gly55Ala)	not specified [RCV004102948]	uncertain significance	22	29308269	29308269	Human		name
156020800	CV2264393	single nucleotide variant	NM_001362985.3(GAS2L1):c.256G>A (p.Ala86Thr)	not specified [RCV004138295]	uncertain significance	22	29308361	29308361	Human		name
155913642	CV2341826	single nucleotide variant	NM_001362985.3(GAS2L1):c.266C>G (p.Ala89Gly)	not specified [RCV004184780]	uncertain significance	22	29308371	29308371	Human		name
401896842	CV2788863	single nucleotide variant	NM_001362985.3(GAS2L1):c.127C>G (p.Leu43Val)	not specified [RCV004362909]	uncertain significance	22	29308232	29308232	Human		name
597780271	CV3680996	single nucleotide variant	NM_001362985.3(GAS2L1):c.179C>T (p.Thr60Met)	not specified [RCV004930616]	uncertain significance	22	29308284	29308284	Human		name
598204461	CV3974137	single nucleotide variant	NM_001362985.3(GAS2L1):c.205G>A (p.Val69Met)	not specified [RCV005337429]	uncertain significance	22	29308310	29308310	Human		name
155978686	CV2215076	single nucleotide variant	NM_001362985.3(GAS2L1):c.967G>A (p.Val323Ile)	not specified [RCV004084845]	likely benign	22	29310955	29310955	Human		name
155981109	CV2244037	single nucleotide variant	NM_001362985.3(GAS2L1):c.349C>G (p.Pro117Ala)	not specified [RCV004108523]	uncertain significance	22	29308454	29308454	Human		name
155958173	CV2282163	single nucleotide variant	NM_001362985.3(GAS2L1):c.967G>T (p.Val323Phe)	not specified [RCV004138893]	uncertain significance	22	29310955	29310955	Human		name
156253278	CV2311444	single nucleotide variant	NM_001362985.3(GAS2L1):c.476A>C (p.Gln159Pro)	not specified [RCV004168289]	uncertain significance	22	29308581	29308581	Human		name
156057910	CV2383304	single nucleotide variant	NM_001362985.3(GAS2L1):c.511G>A (p.Ala171Thr)	not specified [RCV004222348]	uncertain significance	22	29308616	29308616	Human		name
156182107	CV2384135	single nucleotide variant	NM_001362985.3(GAS2L1):c.857C>T (p.Pro286Leu)	not specified [RCV004227538]	uncertain significance	22	29310845	29310845	Human		name
156040948	CV2387666	single nucleotide variant	NM_001362985.3(GAS2L1):c.593C>T (p.Pro198Leu)	not specified [RCV004234211]	uncertain significance	22	29308698	29308698	Human		name
329354031	CV2436811	single nucleotide variant	NM_001362985.3(GAS2L1):c.523C>G (p.Pro175Ala)	not specified [RCV004260211]	uncertain significance	22	29308628	29308628	Human		name
405765320	CV3251461	single nucleotide variant	NM_001362985.3(GAS2L1):c.445C>T (p.Arg149Cys)	not specified [RCV004394978]	uncertain significance	22	29308550	29308550	Human		name
405765334	CV3251463	single nucleotide variant	NM_001362985.3(GAS2L1):c.596G>T (p.Arg199Leu)	not specified [RCV004394980]	uncertain significance	22	29308701	29308701	Human		name
405765340	CV3251464	single nucleotide variant	NM_001362985.3(GAS2L1):c.940C>T (p.Arg314Trp)	not specified [RCV004394981]	uncertain significance	22	29310928	29310928	Human		name
407462364	CV3436459	single nucleotide variant	NM_001362985.3(GAS2L1):c.719C>T (p.Ser240Leu)	not specified [RCV004634528]	uncertain significance	22	29310524	29310524	Human		name
407462367	CV3436460	single nucleotide variant	NM_001362985.3(GAS2L1):c.553A>G (p.Thr185Ala)	not specified [RCV004634529]	uncertain significance	22	29308658	29308658	Human		name
597754702	CV3680998	single nucleotide variant	NM_001362985.3(GAS2L1):c.405C>A (p.Ser135Arg)	not specified [RCV004924437]	uncertain significance	22	29308510	29308510	Human		name
597780275	CV3680999	single nucleotide variant	NM_001362985.3(GAS2L1):c.916A>G (p.Ser306Gly)	not specified [RCV004930617]	uncertain significance	22	29310904	29310904	Human		name
597754707	CV3681000	single nucleotide variant	NM_001362985.3(GAS2L1):c.568G>T (p.Ala190Ser)	not specified [RCV004924438]	uncertain significance	22	29308673	29308673	Human		name
598204438	CV3974133	single nucleotide variant	NM_001362985.3(GAS2L1):c.902G>T (p.Ser301Ile)	not specified [RCV005337425]	uncertain significance	22	29310890	29310890	Human		name
598204444	CV3974134	single nucleotide variant	NM_001362985.3(GAS2L1):c.943G>C (p.Gly315Arg)	not specified [RCV005337426]	uncertain significance	22	29310931	29310931	Human		name
598204455	CV3974136	single nucleotide variant	NM_001362985.3(GAS2L1):c.586C>T (p.Arg196Cys)	not specified [RCV005337428]	uncertain significance	22	29308691	29308691	Human		name
407462370	CV3436461	single nucleotide variant	NM_001362985.3(GAS2L1):c.1013C>T (p.Pro338Leu)	not specified [RCV004634530]	uncertain significance	22	29311464	29311464	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