rs1731641349 Rat Genome Database

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Variant: rs1731641349 -  Homo sapiens

RGD ID: 151884018
RS ID: rs1731641349
ClinVar ID: CV1404908
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GNRHR  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 68,606,365
GRCh38 4 67,740,647
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001012763.2:c.692A>G
NM_000406.3:c.820A>G
NG_009293.1:g.20440A>G
NC_000004.12:g.67740647T>C
More... 		10/30/2021 missense variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:GNRHR
Accession:NM_000406
Location:EXON
Amino Acid Prediction: T to A (nonsynonymous)
Amino Acid Position: 274
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MANSASPEQNQNHCSAINNSIPLMQGNLPTLTLSGKIRVTVTFFLFLLSATFNASFLLKLQKWTQKKEKGKKLSRMKLLL
KHLTLANLLETLIVMPLDGMWNITVQWYAGELLCKVLSYLKLFSMYAPAFMMVVISLDRSLAITRPLALKSNSKVGQSMV
GLAWILSSVFAGPQLYIFRMIHLADSSGQTKVFSQCVTHCSFSQWWHQAFYNFFTFSCLFIIPLFIMLICNAKIIFTLTR
VLHQDPHELQLNQSKNNIPRARLKTLKMTVAFAASFTVCWTPYYVLGIWYWFDPEMLNRLSDPVNHFFFLFAFLNPCFDP
LIYGYFSL*

Gene Symbol:GNRHR
Accession:NM_001012763
Location:EXON
Amino Acid Prediction: H to R (nonsynonymous)
Amino Acid Position: 231
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MANSASPEQNQNHCSAINNSIPLMQGNLPTLTLSGKIRVTVTFFLFLLSATFNASFLLKLQKWTQKKEKGKKLSRMKLLL
KHLTLANLLETLIVMPLDGMWNITVQWYAGELLCKVLSYLKLFSMYAPAFMMVVISLDRSLAITRPLALKSNSKVGQSMV
GLAWILSSVFAGPQLPLHHPSFHHADLQCKNHLHPDTGPSSGPPRTTTESVQEQYTKSTAEDSKNDGCICRFIYCLLDSL
LCPRNLVLV*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV001962247 CLINVAR
dbSNP (RS) rs1731641349 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR