View genomic variant #0000021353

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705526G>T
Published as -
GERP -
Segregation -
DB-ID SLC22A5_000230
MSCV MSCV_0021353
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 0000021353 ./. - - c.-139G>T p.(=) - - - -
SLC22A5 00001144 XM_005272055.1 0000021353 ./. - - c.-139G>T - - - - -
SLC22A5 00001146 XM_005272056.1 0000021353 ./. - - c.-539G>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000327476;
Chromosome 5:131705526..131705526
Allele frequencies from TGP 0.11821
ClinVar Allele ID 300786
Disease database name and identifier MONDO:MONDO:0008919, MedGen:C0342788, OMIM:212140, Orphanet:158
ClinVar preferred disease name Renal carnitine transport defect
HGVS variant names NC 000005.9:g.131705526G>T
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10622510
Gene symbol:Gene id. SLC22A5:6584|MIR3936HG:553103|LOC129994569:129994569
Molecular consequence SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 13180169
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