RGD:597698584 Rat Genome Database

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Variant: RGD:597698584 -  Homo sapiens

RGD ID: 597698584
ClinVar ID: CV3629620
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATG7  VGLL4  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 11,606,450
GRCh38 3 11,564,976
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001284391.1:c.121C>T
NM_014667.4:c.298C>T
NM_001284390.2:c.313C>T
NM_001128219.3:c.316C>T
More... 		11/21/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004885394 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ATG7 CLINVAR
  VGLL4 CLINVAR
OMIM 608760 CLINVAR
  618692 CLINVAR