rs118111581 Rat Genome Database

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Variant: rs118111581 -  Homo sapiens

RGD ID: 14739040
RS ID: rs118111581
ClinVar ID: CV667946
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ETFA  LOC127830280  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 76,603,457
GRCh38 15 76,311,116
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001127716.2:c.39+234G>A
NM_000126.4:c.39+234G>A
NG_007077.2:g.5354G>A
NC_000015.10:g.76311116C>T
More... 		06/14/2018 intron variant likely benign none provided

Gene Symbol:ETFA
Accession:NM_001127716
Location:INTRON

Gene Symbol:ETFA
Accession:NM_000126
Location:INTRON

Gene Symbol:ETFA
Accession:XR_007064434
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV000839685 CLINVAR
dbSNP (RS) rs118111581 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ETFA CLINVAR
OMIM 608053 CLINVAR