RGD:14739204 Rat Genome Database

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Variant: RGD:14739204 -  Homo sapiens

RGD ID: 14739204
RS ID: rs9448857
ClinVar ID: CV662408
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ELOVL4  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 80,628,982
GRCh38 6 79,919,265
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_022726.4:c.669+155T>A
NG_009108.2:g.33334T>A
NC_000006.12:g.79919265A>T
NC_000006.11:g.80628982A>T
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ELOVL4
Accession:NM_022726
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000839767 CLINVAR
dbSNP (RS) rs9448857 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ELOVL4 CLINVAR
OMIM 605512 CLINVAR