RGD:407479298 Rat Genome Database

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Variant: RGD:407479298 -  Homo sapiens

RGD ID: 407479298
ClinVar ID: CV3470289
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PALLD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 169,819,728
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001166109.2:c.1138G>A
NM_001367567.1:c.163G>A
NM_001367569.1:c.163G>A
NM_001367568.1:c.214G>A
More... 		06/22/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004664099 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CBR4 CLINVAR
  PALLD CLINVAR
OMIM 608092 CLINVAR
  619394 CLINVAR