View genomic variant #0000025777

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.172644389C>T
Published as -
GERP -
Segregation -
DB-ID SLC25A12_000040
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00038 View details
Owner Lishuang Shen




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SLC25A12 00001148 NM_003705.4 0000025777 ./. - - c.1654G>A p.(Ala552Thr) - - - -
SLC25A12 00001147 NR_047549.1 0000025777 ./. - - n.1630G>A - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000658888; RCV000765536;
Chromosome 2:172644389..172644389
Allele frequencies from ESP 0.00038
Allele frequencies from ExAC 0.00071
Allele frequencies from TGP 0.00060
ClinVar Allele ID 537369
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0013056, MedGen:C2751855, OMIM:612949, Orphanet:353217
ClinVar preferred disease name not provided|Developmental and epileptic encephalopathy, 39
HGVS variant names NC 000002.11:g.172644389C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SLC25A12:8604
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 142912356
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