RGD:405236667 Rat Genome Database

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Variant: RGD:405236667 -  Homo sapiens

RGD ID: 405236667
ClinVar ID: CV3037973
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANKZF1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 220,099,919
GRCh38 2 219,235,197
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001042410.2:c.1576C>T
NM_018089.3:c.1576C>T
NM_001282792.2:c.946C>T
NC_000002.12:g.219235197C>T
More... 		10/05/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003712354 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ANKZF1 CLINVAR
OMIM 617541 CLINVAR