View genomic variant #0000001046

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.131705698G>A
Published as -
GERP 4.990
Segregation -
DB-ID SLC22A5_000056 See all 2 reported entries
MSCV MSCV_0001046
dbSNP ID rs139203363
Frequency -
Sources ; clinvar; ensembl;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00108 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 0000001046 +/+ - 1/10 c.34G>A p.(Gly12Ser) probably_damaging(0.997) missense_variant - deleterious(0)
SLC22A5 00001144 XM_005272055.1 0000001046 +/+ - 1/10 c.34G>A p.(Gly12Ser) probably_damaging(0.997) missense_variant - deleterious(0)
SLC22A5 00001146 XM_005272056.1 0000001046 +/+ - - c.-367G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000022295; RCV000786404; RCV002298449;
Chromosome 5:131705698..131705698
Allele frequencies from ESP 0.00108
Allele frequencies from ExAC 0.00063
Allele frequencies from TGP 0.00020
ClinVar Allele ID 36683
Disease database name and identifier MONDO:MONDO:0008919, MedGen:C0342788, OMIM:212140, Orphanet:158|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Renal carnitine transport defect|not specified|not provided
HGVS variant names NC 000005.9:g.131705698G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(2)|Uncertain significance(8)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA312960|UniProtKB:O76082#VAR 064109
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 139203363
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