View genomic variant #0000018728

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.36486853G>C
Published as -
GERP -
Segregation -
DB-ID SDHAF1_000005
MSCV MSCV_0018728
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

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SDHAF1 00000294 NM_001042631.2 0000018728 ./. - - c.*329G>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000356291;
Chromosome 19:36486853..36486853
ClinVar Allele ID 343311
Disease database name and identifier MONDO:MONDO:0100294, MedGen:C5700310, OMIM:252011, Orphanet:3208
ClinVar preferred disease name Mitochondrial complex II deficiency, nuclear type 1
HGVS variant names NC 000019.9:g.36486853G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10648566
Gene symbol:Gene id. SDHAF1:644096
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 886054355
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