RGD:15040205 Rat Genome Database

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Variant: RGD:15040205 -  Homo sapiens

RGD ID: 15040205
RS ID: rs1043618
ClinVar ID: CV682503
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HSPA1A  LOC107063610  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 31,783,507
GRCh38 6 31,815,730
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005345.6:c.-27G>C
NG_011855.1:g.4329C>G
NG_046363.1:g.581G>C
NC_000006.12:g.31815730G>C
More...
08/04/2019 5 prime utr variant association Chronic pulmonary obstruction
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:HSPA1A
Accession:NM_005345
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000856576 CLINVAR
dbSNP (RS) rs1043618 CLINVAR
MedGen C0024117 CLINVAR
NCBI Gene 107063610 CLINVAR
  HSPA1A CLINVAR
OMIM 140550 CLINVAR
  606963 CLINVAR