RGD:28870110 Rat Genome Database

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Variant: RGD:28870110 -  Homo sapiens

RGD ID: 28870110
RS ID: rs182429712
ClinVar ID: CV869723
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: YARS2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 32,899,669
GRCh38 12 32,746,735
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001040436.3:c.*469C>T
NC_000012.12:g.32746735G>A
NC_000012.11:g.32899669G>A
NG_028122.1:g.14219C>T
More... 		01/13/2018 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:YARS2
Accession:NM_001040436
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001113410 CLINVAR
dbSNP (RS) rs182429712 CLINVAR
MedGen C3150802 CLINVAR
NCBI Gene YARS2 CLINVAR
OMIM 610957 CLINVAR
  613561 CLINVAR