View genomic variant #0000001065

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705928_131705929insGGCTCGCCACC
Published as -
GERP -
Segregation -
DB-ID SLC22A5_000115
MSCV MSCV_0001065
dbSNP ID -
Frequency -
Sources ;
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 0000001065 ?/? - - c.264_265insGGCTCGCCACC p.(Ile89Glyfs*45) - - - -
SLC22A5 00001144 XM_005272055.1 0000001065 ?/? - - c.264_265insGGCTCGCCACC p.(Ile89Glyfs*45) - - - -
SLC22A5 00001146 XM_005272056.1 0000001065 ?/? - - c.-137_-136insGGCTCGCCACC p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003038905;
Chromosome 5:131705928..131705928
ClinVar Allele ID 2161229
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.131705928C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000688170; RCV002226481;
Chromosome 5:131705929..131705929
ClinVar Allele ID 560154
Disease database name and identifier Human Phenotype Ontology:HP:0003234, MedGen:C1142132|MONDO:MONDO:0008919, MedGen:C0342788, OMIM:212140, Orphanet:158
ClinVar preferred disease name Decreased circulating carnitine concentration|Renal carnitine transport defect
HGVS variant names NC 000005.9:g.131705929A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 765849408
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