RGD:11594323 Rat Genome Database

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Variant: RGD:11594323 -  Homo sapiens

RGD ID: 11594323
RS ID: rs200498239
ClinVar ID: CV296600
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TACR3  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 104,640,842
GRCh38 4 103,719,685
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_023344.1:g.5132A>T
NC_000004.12:g.103719685T>A
NC_000004.11:g.104640842T>A
NM_001059.3:c.-10A>T
More... 		06/14/2016 5 prime utr variant uncertain significance HYPOGONADOTROPIC HYPOGONADISM 11 WITHOUT ANOSMIA
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TACR3
Accession:NM_001059
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000357974 CLINVAR
dbSNP (RS) rs200498239 CLINVAR
MedGen C3553844 CLINVAR
NCBI Gene TACR3 CLINVAR
OMIM 162332 CLINVAR
  614840 CLINVAR