RGD:10046885 Rat Genome Database

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Variant: RGD:10046885 -  Homo sapiens

RGD ID: 10046885
ClinVar ID: CV189365
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: HCN4  LOC105370890  
Reference Nucleotide: -
Variant Nucleotide: TCAC
Position
Assembly Chr Position
GRCh37 15 73,635,725
GRCh38 15 73,343,384
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005477.2:c.1209_1209+1insGTGA
NG_009063.1:g.30880_30881insGTGA
NC_000015.10:g.73343384_73343385insTCAC
NC_000015.9:g.73635725_73635726insTCAC
06/24/2013 splice donor variant likely pathogenic
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:LOC105370890
Accession:NR_188273
Location:EXON;NON-CODING

Gene Symbol:HCN4
Accession:XM_011521148
Location:INTRON

Gene Symbol:HCN4
Accession:NM_005477
Location:INTRON

Variant Samples