RGD:34896068 Rat Genome Database

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Variant: RGD:34896068 -  Homo sapiens

RGD ID: 34896068
RS ID: rs1218350261
ClinVar ID: CV917572
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACSL4  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 108,924,371
GRCh38 X 109,681,142
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001318509.2:c.640-6C>T
NG_008053.1:g.57251C>T
NC_000023.11:g.109681142G>A
NC_000023.10:g.108924371G>A
More... 		10/11/2019 intron variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:ACSL4
Accession:NM_001318510
Location:INTRON

Gene Symbol:ACSL4
Accession:XM_047441919
Location:INTRON

Gene Symbol:FACL4
Accession:NM_004458
Location:INTRON

Gene Symbol:ACSL4
Accession:XM_011530888
Location:INTRON

Gene Symbol:ACSL4
Accession:XM_005262109
Location:INTRON

Gene Symbol:ACSL4
Accession:XM_011530889
Location:INTRON

Gene Symbol:ACSL4
Accession:XM_024452351
Location:INTRON

Gene Symbol:ACSL4
Accession:XM_047441918
Location:INTRON

Gene Symbol:FACL4
Accession:NM_022977
Location:INTRON

Gene Symbol:ACSL4
Accession:NM_001318509
Location:INTRON

Gene Symbol:ACSL4
Accession:XM_006724635
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001193340 CLINVAR
dbSNP (RS) rs1218350261 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ACSL4 CLINVAR
OMIM 300157 CLINVAR