RGD:150407204 Rat Genome Database

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Variant: RGD:150407204 -  Homo sapiens

RGD ID: 150407204
RS ID: rs780986051
ClinVar ID: CV1193406
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TACR3  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 104,579,115
GRCh38 4 103,657,958
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.66859A>C
NC_000004.12:g.103657958T>G
NC_000004.11:g.104579115T>G
NM_001059.3:c.737+257A>C
 12/31/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TACR3
Accession:NM_001059
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001572277 CLINVAR
dbSNP (RS) rs780986051 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TACR3 CLINVAR
OMIM 162332 CLINVAR