RGD:407429653 Rat Genome Database

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Variant: RGD:407429653 -  Homo sapiens

RGD ID: 407429653
ClinVar ID: CV3414040
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAF  WWOX  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 79,246,078
GRCh38 16 79,212,181
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001291997.2:c.*385G>A
NM_016373.4:c.*385G>A
NG_011698.1:g.1117528G>A
NG_016440.2:g.393556C>T
More... 		07/15/2024 3 prime utr variant benign AllHighlyPenetrant

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV004595454 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MAF CLINVAR
  WWOX CLINVAR
OMIM 177075 CLINVAR
  605131 CLINVAR