RGD:408365873 Rat Genome Database

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Variant: RGD:408365873 -  Homo sapiens

RGD ID: 408365873
ClinVar ID: CV3511016
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAF  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 79,633,317
GRCh38 16 79,599,420
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_016440.2:g.6317C>T
NC_000016.10:g.79599420G>A
NC_000016.9:g.79633317G>A
NM_005360.4:c.483C>T
More... 		03/25/2024 synonymous variant likely benign MAF-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004755331 CLINVAR
NCBI Gene MAF CLINVAR
OMIM 177075 CLINVAR