RGD:11596681 Rat Genome Database

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Variant: RGD:11596681 -  Homo sapiens

RGD ID: 11596681
RS ID: rs3733651
ClinVar ID: CV297750
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 186,064,419
GRCh38 4 185,143,265
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_013001.1:g.5003C>T
NC_000004.12:g.185143265C>T
NC_000004.11:g.186064419C>T
LRG_441:g.5003C>T
More... 		06/14/2016 5 prime utr variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000385218 CLINVAR
dbSNP (RS) rs3733651 CLINVAR
MedGen CN294859 CLINVAR
NCBI Gene LOC129993501 CLINVAR
  SLC25A4 CLINVAR
OMIM 103220 CLINVAR