View genomic variant #0000000833

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.74173877T>C
Published as -
GERP 5.680
Segregation -
DB-ID DGUOK_000001 See all 2 reported entries
MSCV MSCV_0000833
dbSNP ID -
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
DGUOK 00000092 NM_080916.1 0000000833 ?/? - 3/5 c.287T>C p.(Leu96Pro) probably_damaging(1) missense_variant - deleterious(0)
DGUOK 00003342 NM_080916.2 0000000833 ?/? - 3/5 c.287T>C p.(Leu96Pro) probably_damaging(1) missense_variant - deleterious(0)
DGUOK 00000093 NM_080918.1 0000000833 ?/? - 3/5 c.287T>C p.(Leu96Pro) probably_damaging(1) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000122730;
Chromosome 2:74173877..74173877
ClinVar Allele ID 139370
Disease database name and identifier MONDO:MONDO:0009636, MedGen:C5191055, OMIM:251880, Orphanet:279934
ClinVar preferred disease name Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
HGVS variant names NC 000002.11:g.74173877T>C
ClinVar review status no assertion criteria provided
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA269923
Gene symbol:Gene id. DGUOK:1716
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant
Allele origin biparental
dbSNP ID 587780587
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