RGD:11589637 Rat Genome Database

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Variant: RGD:11589637 -  Homo sapiens

RGD ID: 11589637
RS ID: rs56012816
ClinVar ID: CV302746
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HOXA1  LOC127408712  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 27,134,003
GRCh38 7 27,094,384
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_011813.1:g.6623C>A
NC_000007.14:g.27094384G>T
NC_000007.13:g.27134003G>T
NM_153620.3:c.*447C>A
More... 		06/19/2021 3 prime utr variant benign|likely benign infancy <1 / 1 000 000 none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:HOXA1
Accession:NM_153620
Location:3UTRS;EXON

Gene Symbol:HOXA1
Accession:NM_005522
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000312312 CLINVAR
  RCV001672691 CLINVAR
dbSNP (RS) rs56012816 CLINVAR
MedGen C1832216 CLINVAR
  C3661900 CLINVAR
NCBI Gene HOXA1 CLINVAR
OMIM 142955 CLINVAR