RGD:405232343 Rat Genome Database

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Variant: RGD:405232343 -  Homo sapiens

RGD ID: 405232343
ClinVar ID: CV3070809
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL27A1  LOC127815673  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 116,997,951
GRCh38 9 114,235,671
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.2619+19C>T
NG_117179.1:g.389C>T
NG_034260.1:g.85127C>T
NC_000009.12:g.114235671C>T
More... 		12/31/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003735018 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL27A1 CLINVAR
OMIM 608461 CLINVAR