RGD:156415027 Rat Genome Database

Variant: RGD:156415027 - Homo sapiens

RGD ID:

156415027

ClinVar ID:

CV1983138

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

GREB1L

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	18	19,075,761
GRCh38	18	21,495,800

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

ClinVar Data

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_001142966.3:c.3146+15A>G NC_000018.10:g.21495800A>G NC_000018.9:g.19075761A>G	04/23/2022	intron variant	likely benign	none provided

Variant Details

Variant Transcripts

Gene Symbol:	GREB1L
Accession:	NM_001142966
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_006722547
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_011526179
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_017025989
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_017025993
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_017025990
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_017025991
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_017025994
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_017025995
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_017025996
Location:	INTRON

Gene Symbol:
Accession:
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437816
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437819
Location:	INTRON

Gene Symbol:
Accession:
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437818
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437809
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437811
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437813
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437815
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437817
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437826
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437824
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437825
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437827
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437821
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437810
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437820
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437814
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	XM_047437822
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	NM_001410867
Location:	INTRON

Gene Symbol:	GREB1L
Accession:	NM_001410868
Location:	INTRON

Variant Samples

ClinVar GRCh37

ClinVar GRCh38

Additional References at PubMed

PMID:28492532

Additional Information

External Database Links

Database	Acc Id	Source(s)
ClinVar	RCV002609477	CLINVAR
MedGen	C3661900	CLINVAR
NCBI Gene	GREB1L	CLINVAR
OMIM	617782	CLINVAR

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)

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Variant: RGD:156415027 - Homo sapiens