View genomic variant #0000016940

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.98987431G>A
Published as -
GERP -
Segregation -
DB-ID SLC25A3_000022
MSCV MSCV_0016940
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 0000016940 ./. - - c.-92G>A p.(=) - - - -
SLC25A3 00001163 NM_005888.3 0000016940 ./. - - c.-92G>A p.(=) - - - -
SLC25A3 00001162 NM_213611.2 0000016940 ./. - - c.-326G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000402654; RCV001552070;
Chromosome 12:98987431..98987431
Allele frequencies from TGP 0.00579
ClinVar Allele ID 318776
Disease database name and identifier MONDO:MONDO:0012557, MedGen:C1835845, OMIM:610773, Orphanet:91130|MedGen:C3661900
ClinVar preferred disease name Cardiomyopathy-hypotonia-lactic acidosis syndrome|not provided
HGVS variant names NC 000012.11:g.98987431G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10633767
Gene symbol:Gene id. SLC25A3:5250
Allele origin germline
dbSNP ID 115763433
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