RGD:13436173 Rat Genome Database

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Variant: RGD:13436173 -  Homo sapiens

RGD ID: 13436173
RS ID: rs1451106951
ClinVar ID: CV433454
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COMP  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 18,899,011
GRCh38 19 18,788,202
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007070.1:g.8104C>T
NC_000019.10:g.18788202G>A
NC_000019.9:g.18899011G>A
NM_000095.3:c.975+10C>T
 02/06/2017 intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:COMP
Accession:NM_000095
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000506702 CLINVAR
dbSNP (RS) rs1451106951 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene COMP CLINVAR
OMIM 600310 CLINVAR