View genomic variant #0000022181

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.158538758C>G
Published as -
GERP -
Segregation -
DB-ID SERAC1_000012
MSCV MSCV_0022181
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.
Legend  

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 0000022181 ./. - - c.1403+1G>C p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000494708;
Chromosome 6:158538758..158538758
ClinVar Allele ID 423258
Disease database name and identifier MONDO:MONDO:0013875, MedGen:C4040739, OMIM:614739, Orphanet:352328
ClinVar preferred disease name 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
HGVS variant names NC 000006.11:g.158538758C>G
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:CA366256718|OMIM:614725.0002
Gene symbol:Gene id. SERAC1:84947
Molecular consequence SO:0001575|splice donor variant
Allele origin germline
dbSNP ID 1131690799
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001946827;
Chromosome 6:158538758..158538758
ClinVar Allele ID 1458175
Disease database name and identifier MONDO:MONDO:0013875, MedGen:C4040739, OMIM:614739, Orphanet:352328
ClinVar preferred disease name 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
HGVS variant names NC 000006.11:g.158538758C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SERAC1:84947
Molecular consequence SO:0001575|splice donor variant
Allele origin germline
dbSNP ID 1131690799
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