RGD:12895901 Rat Genome Database

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Variant: RGD:12895901 -  Homo sapiens

RGD ID: 12895901
RS ID: rs55978915
ClinVar ID: CV390371
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HCN2  LOC107987266  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 610,412
GRCh38 19 610,412
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001194.4:c.1584+7C>T
NG_052810.1:g.25520C>T
NC_000019.10:g.610412C>T
NC_000019.9:g.610412C>T
More... 		03/18/2019 intron variant benign|likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:LOC107987266
Accession:XR_001753828
Location:EXON;NON-CODING

Gene Symbol:HCN2
Accession:NM_001194
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:24033266   PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000454612 CLINVAR
  RCV003970261 CLINVAR
dbSNP (RS) rs55978915 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene HCN2 CLINVAR
OMIM 602781 CLINVAR