View genomic variant #0000021371

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.131705739C>T
Published as -
GERP -
Segregation -
DB-ID SLC22A5_000133
MSCV MSCV_0021371
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00085 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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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 0000021371 ./. - - c.75C>T p.(=) - - - -
SLC22A5 00001144 XM_005272055.1 0000021371 ./. - - c.75C>T - - - - -
SLC22A5 00001146 XM_005272056.1 0000021371 ./. - - c.-326C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000559804;
Chromosome 5:131705739..131705739
Allele frequencies from ESP 0.00085
Allele frequencies from ExAC 0.00017
Allele frequencies from TGP 0.00020
ClinVar Allele ID 454845
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.131705739C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA3403777
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 144054688
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