View genomic variant #0000021156

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.240563C>T
Published as -
GERP -
Segregation -
DB-ID SDHA_000003 See all 2 reported entries
MSCV MSCV_0001011
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00269 View details
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 0000021156 ./. - - c.1523C>T p.(Thr508Ile) - - - -
SDHA 00001116 XM_005248329.1 0000021156 ./. - - c.1523C>T p.(Thr508Ile) - - - -
SDHA 00001119 XM_005248330.1 0000021156 ./. - - c.1379C>T p.(Thr460Ile) - - - -
SDHA 00001115 XM_005248331.1 0000021156 ./. - - c.1523C>T p.(Thr508Ile) - - - -
SDHA 00001117 XR_241710.1 0000021156 ./. - - n.1460C>T - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000032785; RCV000232220; RCV000563852; RCV001719715; RCV001818204;
Chromosome 5:240563..240563
Allele frequencies from ESP 0.00269
Allele frequencies from ExAC 0.00076
Allele frequencies from TGP 0.00140
ClinVar Allele ID 48184
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:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Mitochondrial complex II deficiency, nuclear type 1|Paragangliomas 5|Hereditary cancer-predisposing syndrome|not specified|not provided
HGVS variant names NC 000005.9:g.240563C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(3)|Likely benign(4)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA130381|OMIM:600857.0006
Gene symbol:Gene id. SDHA:6389
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 151266052
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