RGD:150332462 Rat Genome Database

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Variant: RGD:150332462 -  Homo sapiens

RGD ID: 150332462
RS ID: rs17782508
ClinVar ID: CV1172633
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130056092  VRTN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 74,769,841
GRCh38 14 74,303,138
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000014.9:g.74303138C>T
NC_000014.8:g.74769841C>T
NG_032875.1:g.4927G>A
 06/29/2018 benign none provided

Variant Details
Variant Transcripts
Gene Symbol:VRTN
Accession:XM_011536911
Location:5UTRS;EXON

Gene Symbol:VRTN
Accession:NM_018228
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001539047 CLINVAR
dbSNP (RS) rs17782508 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ABCD4 CLINVAR
  LOC130056092 CLINVAR
  VRTN CLINVAR
OMIM 603214 CLINVAR
  620468 CLINVAR