RGD:405207422 Rat Genome Database

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Variant: RGD:405207422 -  Homo sapiens

RGD ID: 405207422
ClinVar ID: CV2909043
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL27A1  LOC124902252  LOC126860736  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 117,050,717
GRCh38 9 114,288,437
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.3988-18C>G
NG_034260.1:g.137893C>G
NG_085236.2:g.825C>G
NC_000009.12:g.114288437C>G
More... 		08/16/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003566685 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL27A1 CLINVAR
  LOC126860736 CLINVAR
OMIM 608461 CLINVAR