View genomic variant #0000025779

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.172725339A>T
Published as -
GERP -
Segregation -
DB-ID SLC25A12_000038
MSCV -
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 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 0000025779 ./. - - c.67-6T>A p.(=) - - - -
SLC25A12 00001147 NR_047549.1 0000025779 ./. - - n.159-6T>A - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000768317;
Chromosome 2:172725339..172725339
ClinVar Allele ID 614233
Disease database name and identifier MONDO:MONDO:0013056, MedGen:C2751855, OMIM:612949, Orphanet:353217
ClinVar preferred disease name Developmental and epileptic encephalopathy, 39
HGVS variant names NC 000002.11:g.172725339A>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SLC25A12:8604
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 1302626614
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001369989;
Chromosome 2:172725340..172725343
ClinVar Allele ID 391511
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.172725342ATAA[2]
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type Microsatellite
Sequence Ontology for variant type SO:0000289
Variant clinical sources reported ClinGen:CA1966485
Gene symbol:Gene id. SLC25A12:8604
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 764075148
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