Rwdd2b Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

30 records found for search term Rwdd2b

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155958391	CV2313780	single nucleotide variant	NM_016940.3(RWDD2B):c.8T>C (p.Ile3Thr)	not specified [RCV004170285]	uncertain significance	21	29019270	29019270	Human		name
156222083	CV2232646	single nucleotide variant	NM_016940.3(RWDD2B):c.17C>T (p.Ser6Phe)	not specified [RCV004101319]	uncertain significance	21	29019261	29019261	Human		name
405700981	CV3310020	single nucleotide variant	NM_016940.3(RWDD2B):c.32A>T (p.Asn11Ile)	not specified [RCV004447098]	uncertain significance	21	29019246	29019246	Human		name
405701009	CV3310025	single nucleotide variant	NM_016940.3(RWDD2B):c.90G>T (p.Met30Ile)	not specified [RCV004447103]	uncertain significance	21	29008599	29008599	Human		name
597733808	CV3597653	single nucleotide variant	NM_016940.3(RWDD2B):c.28T>C (p.Trp10Arg)	not specified [RCV004863368]	uncertain significance	21	29019250	29019250	Human		name
597733814	CV3597654	single nucleotide variant	NM_016940.3(RWDD2B):c.85A>G (p.Lys29Glu)	not specified [RCV004863369]	uncertain significance	21	29008604	29008604	Human		name
597733825	CV3597656	single nucleotide variant	NM_016940.3(RWDD2B):c.47G>C (p.Ser16Thr)	not specified [RCV004863371]	likely benign	21	29019231	29019231	Human		name
8637479	CV92705	single nucleotide variant	NM_016940.2(RWDD2B):c.642C>T (p.Ser214=)	Malignant melanoma [RCV000072803]	not provided	21	29007844	29007844	Human		name
401719516	CV2679559	single nucleotide variant	NM_016940.3(RWDD2B):c.286G>A (p.Glu96Lys)	not specified [RCV004287860]	uncertain significance	21	29008403	29008403	Human		name
401878567	CV2772915	single nucleotide variant	NM_016940.3(RWDD2B):c.169A>G (p.Ile57Val)	not specified [RCV004357686]	uncertain significance	21	29008520	29008520	Human		name
405700968	CV3310018	single nucleotide variant	NM_016940.3(RWDD2B):c.122C>T (p.Ala41Val)	not specified [RCV004447096]	uncertain significance	21	29008567	29008567	Human		name
405700973	CV3310019	single nucleotide variant	NM_016940.3(RWDD2B):c.232G>C (p.Gly78Arg)	not specified [RCV004447097]	uncertain significance	21	29008457	29008457	Human		name
407468718	CV3473230	single nucleotide variant	NM_016940.3(RWDD2B):c.202A>G (p.Lys68Glu)	not specified [RCV004661212]	uncertain significance	21	29008487	29008487	Human		name
597733820	CV3597655	single nucleotide variant	NM_016940.3(RWDD2B):c.296C>T (p.Ala99Val)	not specified [RCV004863370]	likely benign	21	29008306	29008306	Human		name
156097175	CV2253166	single nucleotide variant	NM_016940.3(RWDD2B):c.425A>G (p.Gln142Arg)	not specified [RCV004120935]	uncertain significance	21	29008061	29008061	Human		name
156282032	CV2295165	single nucleotide variant	NM_016940.3(RWDD2B):c.917G>A (p.Cys306Tyr)	not specified [RCV004158262]	uncertain significance	21	29006460	29006460	Human		name
155921665	CV2340493	single nucleotide variant	NM_016940.3(RWDD2B):c.593A>G (p.Tyr198Cys)	not specified [RCV004197217]	uncertain significance	21	29007893	29007893	Human		name
329400608	CV2438558	single nucleotide variant	NM_016940.3(RWDD2B):c.902T>C (p.Leu301Ser)	not specified [RCV004261739]	uncertain significance	21	29006475	29006475	Human		name
329359763	CV2462272	single nucleotide variant	NM_016940.3(RWDD2B):c.497T>G (p.Val166Gly)	not specified [RCV004266267]	uncertain significance	21	29007989	29007989	Human		name
401772637	CV2719705	single nucleotide variant	NM_016940.3(RWDD2B):c.641C>T (p.Ser214Phe)	not specified [RCV004329145]	uncertain significance	21	29007845	29007845	Human		name
401761309	CV2726711	single nucleotide variant	NM_016940.3(RWDD2B):c.923A>T (p.Asp308Val)	not specified [RCV004323044]	uncertain significance	21	29006454	29006454	Human		name
405700987	CV3310021	single nucleotide variant	NM_016940.3(RWDD2B):c.547G>A (p.Val183Ile)	not specified [RCV004447099]	uncertain significance	21	29007939	29007939	Human		name
405700993	CV3310022	single nucleotide variant	NM_016940.3(RWDD2B):c.694C>G (p.Pro232Ala)	not specified [RCV004447100]	uncertain significance	21	29007792	29007792	Human		name
405700999	CV3310023	single nucleotide variant	NM_016940.3(RWDD2B):c.773A>G (p.Asp258Gly)	not specified [RCV004447101]	uncertain significance	21	29006604	29006604	Human		name
405701005	CV3310024	single nucleotide variant	NM_016940.3(RWDD2B):c.893A>G (p.Tyr298Cys)	not specified [RCV004447102]	uncertain significance	21	29006484	29006484	Human		name
407468716	CV3473229	single nucleotide variant	NM_016940.3(RWDD2B):c.616A>G (p.Ile206Val)	not specified [RCV004661211]	uncertain significance	21	29007870	29007870	Human		name
407468721	CV3473231	single nucleotide variant	NM_016940.3(RWDD2B):c.896A>T (p.Gln299Leu)	not specified [RCV004661213]	uncertain significance	21	29006481	29006481	Human		name
598233998	CV3910103	single nucleotide variant	NM_016940.3(RWDD2B):c.761G>T (p.Arg254Leu)	not specified [RCV005274967]	uncertain significance	21	29006616	29006616	Human		name
598234004	CV3910104	single nucleotide variant	NM_016940.3(RWDD2B):c.786T>G (p.Asp262Glu)	not specified [RCV005274968]	uncertain significance	21	29006591	29006591	Human		name
598234010	CV3910105	single nucleotide variant	NM_016940.3(RWDD2B):c.823T>C (p.Ser275Pro)	not specified [RCV005274969]	uncertain significance	21	29006554	29006554	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