View genomic variant #0000019321

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.172691260C>T
Published as -
GERP -
Segregation -
DB-ID SLC25A12_000036
MSCV MSCV_0019321
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01223 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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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 0000019321 ./. - - c.728G>A p.(Arg243Lys) - - - -
SLC25A12 00001147 NR_047549.1 0000019321 ./. - - n.704G>A - - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000676746;
Chromosome 2:172691260..172691260
Allele frequencies from ESP 0.01223
Allele frequencies from ExAC 0.01122
Allele frequencies from TGP 0.00679
ClinVar Allele ID 238387
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.172691260C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1966331
Gene symbol:Gene id. SLC25A12:8604
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 35881803
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