RGD:15152727 Rat Genome Database

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Variant: RGD:15152727 -  Homo sapiens

RGD ID: 15152727
RS ID: rs181462178
ClinVar ID: CV744392
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANLN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 36,462,427
GRCh38 7 36,422,818
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.36422818G>A
NC_000007.13:g.36462427G>A
NM_001284302.3:c.2362+9G>A
NM_018685.5:c.2476+9G>A
More... 		09/19/2019 intron variant benign|likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ANLN
Accession:NM_018685
Location:INTRON

Gene Symbol:ANLN
Accession:XM_017012354
Location:INTRON

Gene Symbol:ANLN
Accession:NM_001284301
Location:INTRON

Gene Symbol:ANLN
Accession:NM_001284302
Location:INTRON

Gene Symbol:ANLN
Accession:XM_017012355
Location:INTRON

Gene Symbol:ANLN
Accession:XM_047420504
Location:INTRON

Gene Symbol:ANLN
Accession:XM_006715747
Location:INTRON

Gene Symbol:ANLN
Accession:XM_017012356
Location:INTRON

Gene Symbol:ANLN
Accession:XM_006715746
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000901625 CLINVAR
  RCV003922979 CLINVAR
dbSNP (RS) rs181462178 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ANLN CLINVAR
OMIM 616027 CLINVAR