RGD:401918790 Rat Genome Database

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Variant: RGD:401918790 -  Homo sapiens

RGD ID: 401918790
ClinVar ID: CV2821361
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACOT9  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 23,725,989
GRCh38 X 23,707,872
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001330259.2:c.523+5A>G
NM_001033583.3:c.703+5A>G
NM_001037171.2:c.730+5A>G
NG_016780.2:g.40419A>G
More... 		03/01/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACOT9
Accession:NM_001033583
Location:INTRON

Gene Symbol:ACOT9
Accession:NM_001037171
Location:INTRON

Gene Symbol:ACOT9
Accession:NM_001330259
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003430452 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACOT9 CLINVAR
OMIM 300862 CLINVAR