RGD:11590092 Rat Genome Database

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Variant: RGD:11590092 -  Homo sapiens

RGD ID: 11590092
RS ID: rs114796827
ClinVar ID: CV302735
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HOXA1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 27,132,714
GRCh38 7 27,093,095
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
NM_005522.5:c.*1345T>C
NG_011813.1:g.7912T>C
NC_000007.14:g.27093095A>G
NC_000007.13:g.27132714A>G
More... 		06/14/2016 3 prime utr variant uncertain significance infancy <1 / 1 000 000
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 RCV000315730 CLINVAR
dbSNP (RS) rs114796827 CLINVAR
MedGen C1832216 CLINVAR
NCBI Gene HOXA1 CLINVAR
OMIM 142955 CLINVAR