Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Modify Subscription
Unsubscribe
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Modify Subscription
Unsubscribe
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
{{ loginError }}
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be sent to {{ username }}
{{geneWatchAttr}}
Analyze
Gene
Strain
QTL
List
×
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)
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
Variant Visualizer
Multi-Ontology Enrichment (MOET)
Gene-Ortholog Location Finder (GOLF)
InterViewer (Protein-Protein Interactions)
PhenoMiner (Quatitative Phenotypes)
Gene Annotator
OLGA (Gene List Generator)
AllianceMine
GViewer (Genome Viewer)
Diseases
Aging & Age-Related Disease
Behavioral & Substance Use Disorder
Cancer & Neoplastic Disease
Cardiovascular Disease
Coronavirus Disease
Developmental Disease
Diabetes
Hematologic Disease
Immune & Inflammatory Disease
Infectious Disease
Liver Disease
Neurological Disease
Obesity & Metabolic Syndrome
Renal Disease
Respiratory Disease
Sensory Organ Disease
Phenotypes & Models
Find Models
Genetic Models
Autism Models
Rat PhenoMiner (Quantitative Phenotypes)
Chinchilla PhenoMiner
Expected Ranges (Quantitative Phenotype)
PhenoMiner Term Comparison
Hybrid Rat Diversity Panel
Phenotypes
Phenotypes in Other Animal Models
Animal Husbandry
Strain Medical Records
Phylogenetics
Strain Availability
Calendar
Rats 101
Submissions
Photo Archive
Pathways
Community
Rat Community Forum
Directory of Rat Laboratories
Video Tutorials
News
RGD Publications
RGD Presentations Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
Variants
search result for
Homo sapiens
(View Results for all Objects and Ontologies)
7
records found for search term
Bag2
Refine Term:
Assembly:
Marshfield Genetic Map
Genethon Genetic Map
Cytogenetic Map
Build 36
Build 34
Celera
TNG Radiation Hybrid Map
deCODE Assembly Map
Stanford-G3 RH Map
GeneMap99-GB4 RH Map
Whitehead-RH Map
Whitehead-YAC Contig Map
NCBI RH Map
GeneMap99-G3 RH Map
GRCh37
HuRef
CRA_TCAGchr7v2
GRCh38
CHM1_1
GRCh38.p14 Ensembl
T2T-CHM13v2.0
Chr
All
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
X
Y
MT
Sort By:
Relevance
RGD ID
Symbol
Variant Type
Name
Trait
Clinical Significance
Chr
Start
Stop
Species
Annotations
Match
Ascending
Descending
Rat
Mouse
Human
All
Export
CSV
TAB
Print
RGD ID
Symbol
Variant Type
Name
Trait
Clinical Significance
Chr
Start
Stop
Species
Annotations
Match
21069376
CV795887
single nucleotide variant
NM_004282.4(
BAG2
):c.222C>T (p.Asp74=)
not provided [RCV000998639]
uncertain significance
6
57182140
57182140
Human
name
156069264
CV2237118
single nucleotide variant
NM_004282.4(
BAG2
):c.92G>T (p.Ser31Ile)
not specified [RCV004114871]
uncertain significance
6
57172789
57172789
Human
name
597741367
CV3631348
single nucleotide variant
NM_004282.4(
BAG2
):c.292G>A (p.Val98Ile)
not specified [RCV004890736]
uncertain significance
6
57183846
57183846
Human
name
156270758
CV2290176
single nucleotide variant
NM_004282.4(
BAG2
):c.364A>G (p.Asn122Asp)
not specified [RCV004152837]
uncertain significance
6
57183918
57183918
Human
name
156129166
CV2358605
single nucleotide variant
NM_004282.4(
BAG2
):c.392C>T (p.Ala131Val)
not specified [RCV004207482]
uncertain significance
6
57183946
57183946
Human
name
598275322
CV3926441
single nucleotide variant
NM_004282.4(
BAG2
):c.550T>G (p.Ser184Ala)
not specified [RCV005304456]
uncertain significance
6
57184104
57184104
Human
name
598275330
CV3926451
single nucleotide variant
NM_004282.4(
BAG2
):c.478A>G (p.Ile160Val)
not specified [RCV005304464]
uncertain significance
6
57184032
57184032
Human
name