View genomic variant #0000019258

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.84650707A>G
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000037
MSCV MSCV_0019258
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 0000019258 ./. - - c.*163T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000301645; RCV000399966; RCV001653627;
Chromosome 2:84650707..84650707
Allele frequencies from TGP 0.80212
ClinVar Allele ID 290971
Disease database name and identifier MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17|MedGen:C3661900|MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698
ClinVar preferred disease name Mitochondrial DNA depletion syndrome 9|not provided|Mitochondrial DNA depletion syndrome
HGVS variant names NC 000002.11:g.84650707A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10616258
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 2832
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