RGD:597669929 Rat Genome Database

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Variant: RGD:597669929 -  Homo sapiens

RGD ID: 597669929
ClinVar ID: CV3661195
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CREB1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 208,435,018
GRCh38 2 207,570,294
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001371428.1:c.358A>G
NM_001320793.2:c.478A>G
NM_001371427.1:c.478A>G
NM_004379.5:c.478A>G
More... 		09/08/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004913009 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CREB1 CLINVAR
OMIM 123810 CLINVAR