RGD:597728347 Rat Genome Database

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Variant: RGD:597728347 -  Homo sapiens

RGD ID: 597728347
ClinVar ID: CV3666809
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DOLK  LOC127816174  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 131,708,941
GRCh38 9 128,946,662
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_744t1:c.642A>G
NM_014908.4:c.642A>G
LRG_744:g.6072A>G
NG_033111.1:g.3970T>C
More... 		10/08/2024 synonymous variant likely benign

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Database
Acc Id
Source(s)
ClinVar RCV004995362 CLINVAR
MedGen CN230736 CLINVAR
NCBI Gene DOLK CLINVAR
OMIM 610746 CLINVAR