View genomic variant #0000001215

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.158567859G>A
Published as -
GERP 3.820
Segregation -
DB-ID SERAC1_000002 See all 2 reported entries
MSCV MSCV_0001215
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

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     
SERAC1 00000295 NM_032861.3 0000001215 ?/? - 6/17 c.442C>T p.(Arg148*) - stop_gained - -
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ClinVar @ MSeqDR

RCVaccession RCV000029218; RCV000414395;
Chromosome 6:158567859..158567859
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 44229
Disease database name and identifier MONDO:MONDO:0013875, MedGen:C3553597, OMIM:614739, Orphanet:ORPHA352328|MedGen:CN517202
ClinVar preferred disease name 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome|not provided
HGVS variant names NC 000006.11:g.158567859G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported OMIM Allelic Variant:614725.0001
Gene symbol:Gene id. SERAC1:84947
Molecular consequence SO:0001587|nonsense, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 387907236
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