View genomic variant #0000021675

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.30886590A>G
Published as -
GERP -
Segregation -
DB-ID VARS2_000007
MSCV MSCV_0021675
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     
VARS2 00001291 NM_001167733.1 0000021675 ./. - - c.566-14A>G p.(=) - - - -
VARS2 00001292 NM_001167734.1 0000021675 ./. - - c.1076-14A>G p.(=) - - - -
VARS2 00001290 NM_020442.4 0000021675 ./. - - c.986-14A>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000625985;
Chromosome 6:30886590..30886590
ClinVar Allele ID 513420
Disease database name and identifier MONDO:MONDO:0014397, MedGen:C4014660, OMIM:615917, Orphanet:420728
ClinVar preferred disease name Combined oxidative phosphorylation defect type 20
HGVS variant names NC 000006.11:g.30886590A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA658796731
Gene symbol:Gene id. VARS2:57176
Molecular consequence SO:0001627|intron variant
Allele origin maternal
dbSNP ID 1297230026
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