rs73417769 Rat Genome Database

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Variant: rs73417769 -  Homo sapiens

RGD ID: 150500346
RS ID: rs73417769
ClinVar ID: CV1235903
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTR9  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 10,787,657
GRCh38 11 10,766,110
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001346279.2:c.1598-292G>A
NM_014633.5:c.1598-292G>A
NG_051671.1:g.20124G>A
NC_000011.10:g.10766110G>A
More... 		04/24/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CTR9
Accession:NM_001346279
Location:INTRON

Gene Symbol:CTR9
Accession:NM_014633
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001656586 CLINVAR
dbSNP (RS) rs73417769 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTR9 CLINVAR
OMIM 609366 CLINVAR