View genomic variant #0000016947

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.98989268G>A
Published as -
GERP -
Segregation -
DB-ID SLC25A3_000001 See all 2 reported entries
MSCV MSCV_0000482
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 0000016947 ./. - - c.158-237G>A p.(=) - - - -
SLC25A3 00001163 NM_005888.3 0000016947 ./. - - c.215G>A p.(Gly72Glu) - - - -
SLC25A3 00001162 NM_213611.2 0000016947 ./. - - c.158-237G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000009720;
Chromosome 12:98989268..98989268
ClinVar Allele ID 24188
Disease database name and identifier MONDO:MONDO:0012557, MedGen:C1835845, OMIM:610773, Orphanet:91130
ClinVar preferred disease name Cardiomyopathy-hypotonia-lactic acidosis syndrome
HGVS variant names NC 000012.11:g.98989268G>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120147|OMIM:600370.0001|UniProtKB:Q00325#VAR 032850
Gene symbol:Gene id. SLC25A3:5250|LOC130008523:130008523
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 104894375
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