View genomic variant #0000020831

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.223625G>A
Published as -
GERP -
Segregation -
DB-ID SDHA_000486
MSCV MSCV_0020831
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 0000020831 ./. - - c.92G>A p.(Arg31Gln) - - - -
SDHA 00001116 XM_005248329.1 0000020831 ./. - - c.92G>A p.(Arg31Gln) - - - -
SDHA 00001119 XM_005248330.1 0000020831 ./. - - c.92G>A p.(Arg31Gln) - - - -
SDHA 00001115 XM_005248331.1 0000020831 ./. - - c.92G>A p.(Arg31Gln) - - - -
SDHA 00001117 XR_241710.1 0000020831 ./. - - n.225G>A - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000225880; RCV000410721; RCV000571153; RCV001589187; RCV002478861; RCV003475078;
Chromosome 5:223625..223625
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 239799
Disease database name and identifier MONDO:MONDO:0100294, MedGen:C5700310, OMIM:252011, Orphanet:3208|MONDO:MONDO:0013602, MedGen:C3279992, OMIM:614165, Orphanet:29072|MONDO:MONDO:0013339, MedGen:C3150898, OMIM:613642, Orphanet:154|MONDO:MONDO:0031006, MedGen:C5543254, OMIM:619259|MONDO:MONDO:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162|MedGen:C3661900
ClinVar preferred disease name Mitochondrial complex II deficiency, nuclear type 1|Paragangliomas 5|Dilated cardiomyopathy 1GG|Neurodegeneration with ataxia and late-onset optic atrophy|Hereditary cancer-predisposing syndrome|not provided
HGVS variant names NC 000005.9:g.223625G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(8)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA3172716
Gene symbol:Gene id. SDHA:6389
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 752532780
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