RGD:11641340 Rat Genome Database

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Variant: RGD:11641340 -  Homo sapiens

RGD ID: 11641340
RS ID: rs767027074
ClinVar ID: CV274188
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HCN4  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 73,614,814
GRCh38 15 73,322,473
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009063.1:g.51792C>T
NC_000015.10:g.73322473G>A
NC_000015.9:g.73614814G>A
NM_005477.3:c.*8C>T
 08/30/2016 3 prime utr variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:HCN4
Accession:XM_011521148
Location:3UTRS;EXON

Gene Symbol:HCN4
Accession:NM_005477
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000353653 CLINVAR
dbSNP (RS) rs767027074 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene HCN4 CLINVAR
OMIM 605206 CLINVAR