RGD:152111924 Rat Genome Database

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Variant: RGD:152111924 -  Homo sapiens

RGD ID: 152111924
RS ID: rs2127545221
ClinVar ID: CV1520552
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZFP57  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 29,641,548
GRCh38 6 29,673,771
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001366333.2:c.137-13T>C
NM_001109809.5:c.353-13T>C
NG_031873.1:g.21791A>G
NG_013045.1:g.8384T>C
More... 		04/17/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ZFP57
Accession:NM_001109809
Location:INTRON

Gene Symbol:ZFP57
Accession:NM_001366333
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002196889 CLINVAR
dbSNP (RS) rs2127545221 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ZFP57 CLINVAR
OMIM 612192 CLINVAR