View genomic variant #0000019314

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.172648078G>A
Published as -
GERP -
Segregation -
DB-ID SLC25A12_000004
MSCV MSCV_0019314
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

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 0000019314 ./. - - c.1468C>T p.(Arg490*) - - - -
SLC25A12 00001147 NR_047549.1 0000019314 ./. - - n.1444C>T p.(Pro482Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001941986;
Chromosome 2:172648078..172648078
ClinVar Allele ID 285227
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.172648078G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SLC25A12:8604
Molecular consequence SO:0001587|nonsense, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 762189046
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