RGD:127233295 Rat Genome Database

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Variant: RGD:127233295 -  Homo sapiens

RGD ID: 127233295
RS ID: rs1442110194
ClinVar ID: CV1094402
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HCN1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 45,303,950
GRCh38 5 45,303,848
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021072.4:c.1378-9C>T
NG_042183.1:g.397271C>T
NC_000005.10:g.45303848G>A
NC_000005.9:g.45303950G>A
06/29/2020 intron variant likely benign Developmental and epileptic encephalopathy; Early infantile epileptic encephalopathy; Ohtahara syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:HCN1
Accession:NM_021072
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001421714 CLINVAR
dbSNP (RS) rs1442110194 CLINVAR
MedGen C0393706 CLINVAR
NCBI Gene HCN1 CLINVAR
OMIM 602780 CLINVAR
SNOMED CT 230429005 CLINVAR