View genomic variant #0000016956

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.98995517T>A
Published as -
GERP -
Segregation -
DB-ID SLC25A3_000016
MSCV MSCV_0016956
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

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SLC25A3 00001164 NM_002635.3 0000016956 ./. - - c.*211T>A p.(=) - - - -
SLC25A3 00001163 NM_005888.3 0000016956 ./. - - c.*211T>A p.(=) - - - -
SLC25A3 00001162 NM_213611.2 0000016956 ./. - - c.*211T>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000385404; RCV001636882;
Chromosome 12:98995517..98995517
Allele frequencies from TGP 0.11981
ClinVar Allele ID 318783
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0012557, MedGen:C1835845, OMIM:610773, Orphanet:91130
ClinVar preferred disease name not provided|Cardiomyopathy-hypotonia-lactic acidosis syndrome
HGVS variant names NC 000012.11:g.98995517T>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10633771
Gene symbol:Gene id. SLC25A3:5250
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 76488843
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