View genomic variant #0000000783

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.36486340G>C
Published as -
GERP 5.670
Segregation -
DB-ID SDHAF1_000001 See all 2 reported entries
MSCV MSCV_0000783
dbSNP ID rs137853193
Frequency -
Sources ; clinVar; Ensembl;
Reference 19465911
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 0000000783 +/+ - 1/1 c.164G>C p.(Arg55Pro) probably_damaging(1) missense_variant - deleterious(0)
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ClinVar @ MSeqDR

RCVaccession RCV000000458;
Chromosome 19:36486340..36486340
ClinVar Allele ID 15469
Disease database name and identifier MONDO:MONDO:0030935, MedGen:C5436933, OMIM:619166
ClinVar preferred disease name Mitochondrial complex 2 deficiency, nuclear type 2
HGVS variant names NC 000019.9:g.36486340G>C
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:CA114273|OMIM:612848.0002|UniProtKB:A6NFY7#VAR 058097
Gene symbol:Gene id. SDHAF1:644096|LOC130064280:130064280
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 137853193
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