rs16956138 Rat Genome Database

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Variant: rs16956138 -  Homo sapiens

RGD ID: 14725131
RS ID: rs16956138
ClinVar ID: CV668225
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC13A5  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 6,591,067
GRCh38 17 6,687,748
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_177550.5:c.1438-82A>G
NM_001284510.2:c.1309-82A>G
NM_001284509.2:c.1387-82A>G
NM_001143838.3:c.1438-1410A>G
More... 		06/14/2018 intron variant benign none provided

Gene Symbol:SLC13A5
Accession:XM_011523795
Location:3UTRS;EXON

Gene Symbol:SLC13A5
Accession:NM_001143838
Location:INTRON

Gene Symbol:SLC13A5
Accession:NM_001284510
Location:INTRON

Gene Symbol:SLC13A5
Accession:NM_177550
Location:INTRON

Gene Symbol:SLC13A5
Accession:NM_001284509
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV000833298 CLINVAR
dbSNP (RS) rs16956138 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC13A5 CLINVAR
OMIM 608305 CLINVAR