RGD:405156361 Rat Genome Database

RGD:405156361 Rat Genome Database

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Variant: RGD:405156361 - Homo sapiens

RGD ID:

405156361

ClinVar ID:

CV2950846

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

Reference Nucleotide:

G

Variant Nucleotide:

A

Position

Assembly	Chr	Position
GRCh37	4	68,610,500
GRCh38	4	67,744,782

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_001012763.2:c.523-123C>T NM_000406.3:c.528C>T NG_009293.1:g.16305C>T NC_000004.12:g.67744782G>A More...	03/29/2023	intron variant	likely benign	none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:	GNRHR
Accession:	NM_000406
Location:	EXON
Amino Acid Prediction:	Y to Y (synonymous)
Amino Acid Position:	176

Amino Acid Sequence (Calculated using NCBI transcript definition)
MANSASPEQNQNHCSAINNSIPLMQGNLPTLTLSGKIRVTVTFFLFLLSATFNASFLLKLQKWTQKKEKGKKLSRMKLLL KHLTLANLLETLIVMPLDGMWNITVQWYAGELLCKVLSYLKLFSMYAPAFMMVVISLDRSLAITRPLALKSNSKVGQSMV GLAWILSSVFAGPQLYIFRMIHLADSSGQTKVFSQCVTHCSFSQWWHQAFYNFFTFSCLFIIPLFIMLICNAKIIFTLTR VLHQDPHELQLNQSKNNIPRARLKTLKMTVAFATSFTVCWTPYYVLGIWYWFDPEMLNRLSDPVNHFFFLFAFLNPCFDP LIYGYFSL*

Gene Symbol:	GNRHR
Accession:	NM_001012763
Location:	INTRON

ClinVar GRCh37	ClinVar GRCh38

PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV003670352	CLINVAR
MedGen	C3661900	CLINVAR
NCBI Gene	GNRHR	CLINVAR
OMIM	138850	CLINVAR