View genomic variant #0000019271

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.84668557A>G
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000032
MSCV MSCV_0019271
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00062 View details
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     

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DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SUCLG1 00000316 NM_003849.3 0000019271 ./. - - c.345T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000290324; RCV000345295; RCV001718713;
Chromosome 2:84668557..84668557
Allele frequencies from ESP 0.00062
Allele frequencies from ExAC 0.00032
ClinVar Allele ID 288079
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MedGen:C3661900|MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name Mitochondrial DNA depletion syndrome|not provided|Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84668557A>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1736329
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 374594774
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