RGD:407488633 Rat Genome Database

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Variant: RGD:407488633 -  Homo sapiens

RGD ID: 407488633
ClinVar ID: CV3421584
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACOT2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 74,036,498
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000014.9:g.73569794C>G
NC_000014.8:g.74036498C>G
NM_006821.4:c.554C>G
NP_001351107.1:p.Thr185Arg
More... 		05/22/2024 intron variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004604009 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ACOT2 CLINVAR
  HEATR4 CLINVAR
OMIM 609972 CLINVAR