View genomic variant #0000000838

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.84668393G>C
Published as -
GERP 5.590
Segregation -
DB-ID SUCLG1_000001 See all 2 reported entries
MSCV MSCV_0000838
dbSNP ID rs267607099
Frequency -
Sources ; clinVar; Ensembl;
Reference 20693550
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 0000000838 +/+ - 4/9 c.509C>G p.(Pro170Arg) probably_damaging(1) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000001041;
Chromosome 2:84668393..84668393
ClinVar Allele ID 33449
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.84668393G>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA114698|OMIM:611224.0003|UniProtKB:P53597#VAR 065121
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 267607099
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