RGD:150467072 Rat Genome Database

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Variant: RGD:150467072 -  Homo sapiens

RGD ID: 150467072
RS ID: rs10245096
ClinVar ID: CV1277509
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GHRHR  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 31,015,879
GRCh38 7 30,976,264
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000823.4:c.975-165G>A
NG_021416.1:g.17244G>A
NC_000007.14:g.30976264G>A
NC_000007.13:g.31015879G>A
06/21/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GHRHR
Accession:NM_000823
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001710804 CLINVAR
dbSNP (RS) rs10245096 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GHRHR CLINVAR
OMIM 139191 CLINVAR