RGD:407461046 Rat Genome Database

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Variant: RGD:407461046 -  Homo sapiens

RGD ID: 407461046
ClinVar ID: CV3488488
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF175  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 52,091,638
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000019.10:g.51588385A>G
NC_000019.9:g.52091638A>G
NM_007147.2:c.2054A>G
NP_009078.1:p.Asn685Ser
More...
05/01/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004687555 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ZNF175 CLINVAR
OMIM 601139 CLINVAR