RGD:152044901 Rat Genome Database

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Variant: RGD:152044901 -  Homo sapiens

RGD ID: 152044901
RS ID: rs771588323
ClinVar ID: CV1584496
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC22A5  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 131,729,351
GRCh38 5 132,393,659
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003060.4:c.1451-17C>T
NM_001308122.2:c.1523-17C>T
NG_008982.2:g.28956C>T
NC_000005.10:g.132393659C>T
More... 		05/02/2021 intron variant likely benign Carnitine Deficiency, Systemic; Carnitine deficiency, systemic, due to defect in renal reabsorption of carnitine; Carnitine plasma-membrane transporter deficiency; Carnitine transporter deficiency; CARNITINE TRANSPORTER, PLASMA-MEMBRANE, DEFICIENCY OF; Carnitine uptake defect; Primary carnitine deficiency; Systemic primary carnitine deficiency disease
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC22A5
Accession:XM_047417597
Location:INTRON

Gene Symbol:SLC22A5
Accession:XM_047417598
Location:INTRON

Gene Symbol:SLC22A5
Accession:XM_047417596
Location:INTRON

Gene Symbol:SLC22A5
Accession:XM_047417595
Location:INTRON

Gene Symbol:SLC22A5
Accession:NM_003060
Location:INTRON

Gene Symbol:SLC22A5
Accession:XM_011543590
Location:INTRON

Gene Symbol:SLC22A5
Accession:XM_017009778
Location:INTRON

Gene Symbol:SLC22A5
Accession:NM_001308122
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002071481 CLINVAR
dbSNP (RS) rs771588323 CLINVAR
MedGen C0342788 CLINVAR
NCBI Gene SLC22A5 CLINVAR
OMIM 212140 CLINVAR
  603377 CLINVAR
SNOMED CT 21764004 CLINVAR