RGD:12843034 Rat Genome Database

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Variant: RGD:12843034 -  Homo sapiens

RGD ID: 12843034
RS ID: rs370312170
ClinVar ID: CV372290
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOXRED1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 126,143,358
GRCh38 11 126,273,463
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_028029.1:g.9424C>G
NC_000011.10:g.126273463C>G
NC_000011.9:g.126143358C>G
NM_017547.4:c.536+9C>G
More... 		09/17/2021 intron variant benign|likely benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:FOXRED1
Accession:XM_047427253
Location:5UTRS;INTRON

Gene Symbol:FOXRED1
Accession:XM_017018000
Location:INTRON

Gene Symbol:FOXRED1
Accession:XM_017018002
Location:INTRON

Gene Symbol:FOXRED1
Accession:XM_047427252
Location:INTRON

Gene Symbol:FOXRED1
Accession:XM_006718879
Location:INTRON

Gene Symbol:FOXRED1
Accession:NM_017547
Location:INTRON

Gene Symbol:FOXRED1
Accession:NR_037647
Location:INTRON;NON-CODING

Gene Symbol:FOXRED1
Accession:NR_037648
Location:INTRON;NON-CODING

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


Additional Information

Database Acc Id Source(s)
ClinVar RCV000435501 CLINVAR
  RCV002063597 CLINVAR
  RCV003912774 CLINVAR
dbSNP (RS) rs370312170 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene FOXRED1 CLINVAR
OMIM 613622 CLINVAR