Apod Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

22 records found for search term Apod

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8578536	CV112920	single nucleotide variant	NM_001647.3(APOD):c.334+239G>C	Lung cancer [RCV000093443]	uncertain significance	3	195571038	195571038	Human		name
8578537	CV112921	single nucleotide variant	NM_001647.3(APOD):c.124-2165C>G	Lung cancer [RCV000093444]	uncertain significance	3	195576136	195576136	Human		name
8578538	CV112922	single nucleotide variant	NM_001647.3(APOD):c.-34-1226G>T	Lung cancer [RCV000093445]	uncertain significance	3	195580721	195580721	Human		name
15160322	CV748156	single nucleotide variant	NM_001647.4(APOD):c.165C>A (p.Thr55=)	not provided [RCV000925461]	likely benign	3	195573930	195573930	Human		name
156221084	CV2222453	single nucleotide variant	NM_001647.4(APOD):c.31C>G (p.Leu11Val)	not specified [RCV004099307]	uncertain significance	3	195579431	195579431	Human		name
156004161	CV2357537	single nucleotide variant	NM_001647.4(APOD):c.85C>T (p.Pro29Ser)	not specified [RCV004202811]	uncertain significance	3	195579377	195579377	Human		name
405662624	CV3289885	single nucleotide variant	NM_001647.4(APOD):c.74T>C (p.Leu25Pro)	not specified [RCV004417830]	uncertain significance	3	195579388	195579388	Human		name
15165765	CV697996	single nucleotide variant	NM_001647.4(APOD):c.44T>C (p.Phe15Ser)	APOD-related disorder [RCV003895753]\|not provided [RCV000948671]	benign	3	195579418	195579418	Human	2	name , trait , alternate_id
15165765	CV697996	single nucleotide variant	NM_001647.4(APOD):c.44T>C (p.Phe15Ser)	APOD-related disorder [RCV003895753]\|not provided [RCV000948671]	benign	3	195579418	195579419	Human	2	name , trait , alternate_id
155914221	CV2341950	single nucleotide variant	NM_001647.4(APOD):c.142G>A (p.Glu48Lys)	not specified [RCV004184894]	uncertain significance	3	195573953	195573953	Human		name
401781026	CV2681866	single nucleotide variant	NM_001647.4(APOD):c.178C>T (p.Arg60Cys)	not specified [RCV004296860]	uncertain significance	3	195573917	195573917	Human		name
401927656	CV2825150	single nucleotide variant	NM_001647.4(APOD):c.226G>A (p.Val76Met)	not provided [RCV003439098]	benign	3	195573869	195573869	Human		name
405258464	CV3203829	single nucleotide variant	NM_001647.4(APOD):c.166T>G (p.Phe56Val)	APOD-related disorder [RCV003941998]	benign	3	195573929	195573929	Human		name , trait , alternate_id
405662619	CV3289883	single nucleotide variant	NM_001647.4(APOD):c.160A>C (p.Thr54Pro)	not specified [RCV004417828]	uncertain significance	3	195573935	195573935	Human		name
405662622	CV3289884	single nucleotide variant	NM_001647.4(APOD):c.274G>C (p.Gly92Arg)	not specified [RCV004417829]	uncertain significance	3	195571337	195571337	Human		name
597678037	CV3572405	single nucleotide variant	NM_001647.4(APOD):c.157C>T (p.Pro53Ser)	not specified [RCV004837059]	uncertain significance	3	195573938	195573938	Human		name
155982943	CV2347843	single nucleotide variant	NM_001647.4(APOD):c.559A>G (p.Lys187Glu)	not specified [RCV004195495]	likely benign	3	195568911	195568911	Human		name
156339472	CV2351587	single nucleotide variant	NM_001647.4(APOD):c.304C>G (p.Pro102Ala)	not specified [RCV004195306]	uncertain significance	3	195571307	195571307	Human		name
156221103	CV2397413	single nucleotide variant	NM_001647.4(APOD):c.370G>A (p.Asp124Asn)	not specified [RCV004238932]	uncertain significance	3	195569100	195569100	Human		name
329374113	CV2443658	single nucleotide variant	NM_001647.4(APOD):c.350C>T (p.Pro117Leu)	not specified [RCV004255963]	uncertain significance	3	195569120	195569120	Human		name
405283650	CV3191782	single nucleotide variant	NM_001647.4(APOD):c.383A>G (p.Tyr128Cys)	APOD-related disorder [RCV003921882]	likely benign	3	195569087	195569087	Human		name , trait , alternate_id
597677935	CV3572395	single nucleotide variant	NM_001647.4(APOD):c.531G>A (p.Met177Ile)	not specified [RCV004837049]	uncertain significance	3	195568939	195568939	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