RGD:150447481 Rat Genome Database

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Variant: RGD:150447481 -  Homo sapiens

RGD ID: 150447481
RS ID: rs350130
ClinVar ID: CV1261825
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KISS1R  LOC127889820  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 919,656
GRCh38 19 919,656
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032551.5:c.505+31A>G
NG_008277.1:g.7315A>G
NC_000019.10:g.919656A>G
NC_000019.9:g.919656A>G
 09/22/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KISS1R
Accession:NM_032551
Location:INTRON

Gene Symbol:KISS1R
Accession:XM_047439545
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001680209 CLINVAR
dbSNP (RS) rs350130 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KISS1R CLINVAR
OMIM 604161 CLINVAR