View genomic variant #0000020805

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.218408G>A
Published as -
GERP -
Segregation -
DB-ID SDHA_000371
MSCV MSCV_0020805
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

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SDHA 00001118 NM_004168.2 0000020805 ./. - - c.-63G>A p.(=) - - - -
SDHA 00001116 XM_005248329.1 0000020805 ./. - - c.-63G>A p.(=) - - - -
SDHA 00001119 XM_005248330.1 0000020805 ./. - - c.-63G>A p.(=) - - - -
SDHA 00001115 XM_005248331.1 0000020805 ./. - - c.-63G>A p.(=) - - - -
SDHA 00001117 XR_241710.1 0000020805 ./. - - n.71G>A - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000272151; RCV000329506; RCV000364389;
Chromosome 5:218408..218408
ClinVar Allele ID 299305
Disease database name and identifier Human Phenotype Ontology:HP:0002666, MONDO:MONDO:0008233, MedGen:C0031511, OMIM:171300, Orphanet:29072|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0100294, MedGen:C5700310, OMIM:252011, Orphanet:3208
ClinVar preferred disease name Pheochromocytoma|Leigh syndrome|Mitochondrial complex II deficiency, nuclear type 1
HGVS variant names NC 000005.9:g.218408G>A
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:CA10621607
Gene symbol:Gene id. SDHA:6389
Allele origin germline
dbSNP ID 886060513
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