View genomic variant #0000019283

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.84676890_84676891insGGTT
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000011
MSCV MSCV_0019283
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.
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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 0000019283 ./. - - c.98-15_98-14insAACC p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000295211; RCV000350089;
Chromosome 2:84676890..84676891
ClinVar Allele ID 290736
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.84676890 84676891insGGTT
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Insertion
Sequence Ontology for variant type SO:0000667
Variant clinical sources reported ClinGen:CA10616104
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 886056352
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