View genomic variant #0000021372

Chromosome 5
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705747G>T
Published as -
GERP -
Segregation -
DB-ID SLC22A5_000063 See all 2 reported entries
MSCV MSCV_0001053
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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 0000021372 ./. - - c.83G>T p.(Ser28Ile) - - - -
SLC22A5 00001144 XM_005272055.1 0000021372 ./. - - c.83G>T - - - - -
SLC22A5 00001146 XM_005272056.1 0000021372 ./. - - c.-318G>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000022301; RCV001549353;
Chromosome 5:131705747..131705747
ClinVar Allele ID 36688
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0008919, MedGen:C0342788, OMIM:212140, Orphanet:158
ClinVar preferred disease name not provided|Renal carnitine transport defect
HGVS variant names NC 000005.9:g.131705747G>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA342613
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 72552724
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