rs1583619560 Rat Genome Database

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Variant: rs1583619560 - Homo sapiens

RGD ID:

25319327

RS ID:

rs1583619560

ClinVar ID:

CV817073

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

OPRM1

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	6	154,440,078
GRCh38	6	154,118,943

JBrowse:

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Model

Annotation Click to see Annotation Detail View

ClinVar Data

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
LRG_1007t1:c.1164+27471G>A LRG_1007t2:c.222G>A NM_000914.5:c.222G>A NM_001285522.1:c.*257G>A More...	04/28/2018	3 prime utr variant	drug response	Ultram response

Variant Details

Variant Transcripts

Gene Symbol:	OPRM1
Accession:	NM_000914
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NM_001285526
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NM_001145279
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NM_001145280
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NM_001145287
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NM_001145281
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NM_001285522
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NM_001285524
Location:	3UTRS;EXON

Gene Symbol:	OPRM1
Accession:	NR_104348
Location:	EXON;NON-CODING

Gene Symbol:	OPRM1
Accession:	NR_104350
Location:	EXON;NON-CODING

Gene Symbol:	OPRM1
Accession:	XM_017010904
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001145282
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001145284
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001285523
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	XM_011535851
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001008503
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001145285
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	XM_011535856
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001008505
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001285528
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001145286
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001008504
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	XM_017010907
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	XM_011535853
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	XM_017010903
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	XM_047418837
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001145283
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NM_001285527
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	XM_011535862
Location:	INTRON

Gene Symbol:	OPRM1
Accession:	NR_104349
Location:	INTRON;NON-CODING

Gene Symbol:	OPRM1
Accession:	NR_104351
Location:	INTRON;NON-CODING

Variant Samples

ClinVar GRCh37

ClinVar GRCh38

Additional Information

External Database Links

Database	Acc Id	Source(s)
ClinVar	RCV001028196	CLINVAR
dbSNP (RS)	rs1583619560	CLINVAR
MedGen	CN078023	CLINVAR
NCBI Gene	OPRM1	CLINVAR
OMIM	600018	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: rs1583619560 - Homo sapiens