RGD:405235228 Rat Genome Database

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Variant: RGD:405235228 -  Homo sapiens

RGD ID: 405235228
ClinVar ID: CV3166234
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL27A1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 117,062,892
GRCh38 9 114,300,612
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032888.4:c.4639-13C>T
NG_034260.1:g.150068C>T
NC_000009.12:g.114300612C>T
NC_000009.11:g.117062892C>T
 01/18/2024 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003853683 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL27A1 CLINVAR
OMIM 608461 CLINVAR