View genomic variant #0000019262

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.84650883C>G
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000005
MSCV MSCV_0019262
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

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SUCLG1 00000316 NM_003849.3 0000019262 ./. - - c.1028G>C p.(Arg343Thr) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000274138; RCV000368206;
Chromosome 2:84650883..84650883
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 290733
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name Mitochondrial DNA depletion syndrome|Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84650883C>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:CA1736111
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 748995693
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