RGD:13442551 Rat Genome Database

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Variant: RGD:13442551 -  Homo sapiens

RGD ID: 13442551
RS ID: rs12406470
ClinVar ID: CV417642
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MIR181A1HG  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 198,796,120
GRCh38 1 198,826,991
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000001.11:g.198826991C>T
NC_000001.10:g.198796120C>T
 10/28/2020 pathogenic|benign Acute myeloid leukemia with maturation; AllHighlyPenetrant
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MIR181A1HG
Accession:NR_040073
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:29254171   PMID:33116287  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000509076 CLINVAR
  RCV001777166 CLINVAR
dbSNP (RS) rs12406470 CLINVAR
MedGen C1879321 CLINVAR
  CN169374 CLINVAR
NCBI Gene MIR181A1HG CLINVAR