RGD:12838898 Rat Genome Database

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Variant: RGD:12838898 -  Homo sapiens

RGD ID: 12838898
RS ID: rs191769818
ClinVar ID: CV371702
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYC1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 145,151,231
GRCh38 8 144,096,328
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_033872.1:g.6294C>T
NC_000008.11:g.144096328C>T
NC_000008.10:g.145151231C>T
NM_001916.5:c.454-9C>T
More... 		11/12/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CYC1
Accession:NM_001916
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000676779 CLINVAR
dbSNP (RS) rs191769818 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CYC1 CLINVAR
OMIM 123980 CLINVAR