View genomic variant #0000021369

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705723T>A
Published as -
GERP -
Segregation -
DB-ID SLC22A5_000060 See all 2 reported entries
MSCV MSCV_0001050
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.005 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SLC22A5 00001145 NM_003060.3 0000021369 ./. - - c.59T>A p.(Leu20His) - - - -
SLC22A5 00001144 XM_005272055.1 0000021369 ./. - - c.59T>A - - - - -
SLC22A5 00001146 XM_005272056.1 0000021369 ./. - - c.-342T>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000022299; RCV000838010; RCV001194405;
Chromosome 5:131705723..131705723
Allele frequencies from ESP 0.00500
Allele frequencies from ExAC 0.00136
Allele frequencies from TGP 0.00359
ClinVar Allele ID 36686
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0008919, MedGen:C0342788, OMIM:212140, Orphanet:158|MedGen:CN169374
ClinVar preferred disease name not provided|Renal carnitine transport defect|not specified
HGVS variant names NC 000005.9:g.131705723T>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(5)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA342609
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 144020613
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None