RGD:407573113 Rat Genome Database

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Variant: RGD:407573113 -  Homo sapiens

RGD ID: 407573113
ClinVar ID: CV3498913
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAF  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 79,628,388
GRCh38 16 79,594,491
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005360.5:c.1181A>T
NM_001031804.3:c.*4290A>T
NG_016440.1:g.11235A>T
NG_016440.2:g.11246A>T
More... 		06/10/2024 3 prime utr variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004699883 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MAF CLINVAR
OMIM 177075 CLINVAR