RGD:405142766 Rat Genome Database

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Variant: RGD:405142766 -  Homo sapiens

RGD ID: 405142766
ClinVar ID: CV3126019
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL27A1  LOC105376224  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 117,066,947
GRCh38 9 114,304,667
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.4932G>A
NG_034260.1:g.154123G>A
NC_000009.12:g.114304667G>A
NC_000009.11:g.117066947G>A
More... 		01/27/2024 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003816935 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL27A1 CLINVAR
OMIM 608461 CLINVAR