RGD:408388926 Rat Genome Database

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Variant: RGD:408388926 -  Homo sapiens

RGD ID: 408388926
ClinVar ID: CV3522825
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126805688  YARS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 33,252,552
GRCh38 1 32,786,951
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_273t1:c.809C>T
NM_003680.4:c.809C>T
LRG_273:g.36082C>T
NG_008408.1:g.36082C>T
More... 		10/30/2023 missense variant uncertain significance none provided

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Database
Acc Id
Source(s)
ClinVar RCV004769206 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126805688 CLINVAR
  YARS1 CLINVAR
OMIM 603623 CLINVAR