View genomic variant #0000017274

Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.48516791_48516792insC
Published as -
GERP -
Segregation -
DB-ID SUCLA2_000042
MSCV MSCV_0017274
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

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SUCLA2 00000313 NM_003850.2 0000017274 ./. - - c.*714_*715insG p.(=) - - - -
SUCLA2 00000312 XM_005266579.1 0000017274 ./. - - c.*714_*715insG - - - - -
SUCLA2 00000315 XM_005266580.1 0000017274 ./. - - c.*714_*715insG - - - - -
SUCLA2 00000314 XM_005266581.1 0000017274 ./. - - c.*714_*715insG p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000399206;
Chromosome 13:48516791..48516792
Allele frequencies from TGP 0.00599
ClinVar Allele ID 334869
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698
ClinVar preferred disease name Mitochondrial DNA depletion syndrome
HGVS variant names NC 000013.10:g.48516792dup
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA10643539
Gene symbol:Gene id. SUCLA2:8803
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 563064046
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