RGD:28901147 Rat Genome Database

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Variant: RGD:28901147 -  Homo sapiens

RGD ID: 28901147
RS ID: rs183965171
ClinVar ID: CV867111
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC37A4  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 118,895,357
GRCh38 11 119,024,647
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_013331.1:g.11259T>C
NC_000011.10:g.119024647A>G
NC_000011.9:g.118895357A>G
LRG_187t1:c.*263T>C
More... 		01/13/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC37A4
Accession:NM_001164278
Location:3UTRS;EXON

Gene Symbol:SLC37A4
Accession:NM_001467
Location:3UTRS;EXON

Gene Symbol:SLC37A4
Accession:NM_001164277
Location:3UTRS;EXON

Gene Symbol:SLC37A4
Accession:NM_001164280
Location:3UTRS;EXON

Gene Symbol:SLC37A4
Accession:NM_001164279
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001104112 CLINVAR
dbSNP (RS) rs183965171 CLINVAR
MedGen C0017920 CLINVAR
NCBI Gene SLC37A4 CLINVAR
OMIM 602671 CLINVAR
SNOMED CT 7265005 CLINVAR