RGD:15115330 Rat Genome Database

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Variant: RGD:15115330 -  Homo sapiens

RGD ID: 15115330
RS ID: rs143133700
ClinVar ID: CV695896
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CCNQ  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 152,859,997
GRCh38 X 153,594,539
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008393.2:g.9639C>T
NC_000023.11:g.153594539G>A
NC_000023.10:g.152859997G>A
NM_152274.3:c.429+8C>T
More... 		12/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CCNQ
Accession:NM_152274
Location:INTRON

Gene Symbol:CCNQ
Accession:XM_011531214
Location:INTRON

Gene Symbol:CCNQ
Accession:XM_047442631
Location:INTRON

Gene Symbol:CCNQ
Accession:NM_001130997
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000873120 CLINVAR
dbSNP (RS) rs143133700 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CCNQ CLINVAR
OMIM 300708 CLINVAR