RGD:401935220 Rat Genome Database

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Variant: RGD:401935220 -  Homo sapiens

RGD ID: 401935220
ClinVar ID: CV2805518
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATAD3A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 1,469,314
GRCh38 1 1,533,934
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001170536.3:c.1386G>A
NM_001170535.3:c.1623G>A
NM_018188.5:c.1767G>A
NG_041807.1:g.11427C>T
More... 		01/01/2023 synonymous variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

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Database
Acc Id
Source(s)
ClinVar RCV003412643 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ATAD3A CLINVAR
OMIM 612316 CLINVAR