View genomic variant #0000001047

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705707G>T
Published as -
GERP 4.990
Segregation -
DB-ID SLC22A5_000057 See all 2 reported entries
MSCV MSCV_0001047
dbSNP ID rs267607052
Frequency -
Sources ; clinvar; ensembl;
Reference 20027113
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 0000001047 +/+ - 1/10 c.43G>T p.(Gly15Trp) probably_damaging(0.999) missense_variant - deleterious(0)
SLC22A5 00001144 XM_005272055.1 0000001047 +/+ - 1/10 c.43G>T p.(Gly15Trp) probably_damaging(0.999) missense_variant - deleterious(0)
SLC22A5 00001146 XM_005272056.1 0000001047 +/+ - - c.-358G>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006798; RCV000186150;
Chromosome 5:131705707..131705707
Allele frequencies from ExAC 0.00010
ClinVar Allele ID 21468
Disease database name and identifier MedGen:C3661900|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.131705707G>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA312963|OMIM:603377.0022|UniProtKB:O76082#VAR 064110
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 267607052
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