View genomic variant #0000019267

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.84668395del
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000029
MSCV MSCV_0019267
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 0000019267 ./. - - c.507del p.(Asn171Thrfs*35) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000193104;
Chromosome 2:84668395..84668395
ClinVar Allele ID 207028
Disease database name and identifier MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84668397del
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA206365
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 797046017
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