RGD:150445663 Rat Genome Database

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Variant: RGD:150445663 -  Homo sapiens

RGD ID: 150445663
RS ID: rs7612
ClinVar ID: CV1248341
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACTB  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 5,567,112
GRCh38 7 5,527,481
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001101.5:c.*267G>A
LRG_132:g.8121G>A
NG_007992.1:g.8121G>A
NC_000007.13:g.5567112C>T
More... 		08/15/2019 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACTB
Accession:NM_001101
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001667048 CLINVAR
dbSNP (RS) rs7612 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACTB CLINVAR
OMIM 102630 CLINVAR