RGD:127290136 Rat Genome Database

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Variant: RGD:127290136 -  Homo sapiens

RGD ID: 127290136
RS ID: rs190879861
ClinVar ID: CV1156377
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HTRA1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 124,269,687
GRCh38 10 122,510,171
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002775.5:c.1178+18G>A
NG_011554.1:g.53647G>A
NC_000010.11:g.122510171G>A
NC_000010.10:g.124269687G>A
 10/28/2020 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HTRA1
Accession:NM_002775
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001509661 CLINVAR
dbSNP (RS) rs190879861 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HTRA1 CLINVAR
OMIM 602194 CLINVAR