View genomic variant #0000020889

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.225663G>A
Published as -
GERP -
Segregation -
DB-ID SDHA_000220
MSCV MSCV_0020889
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 View details
Owner LOVD




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
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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 0000020889 ./. - - c.442G>A p.(Ala148Thr) - - - -
SDHA 00001116 XM_005248329.1 0000020889 ./. - - c.442G>A p.(Ala148Thr) - - - -
SDHA 00001119 XM_005248330.1 0000020889 ./. - - c.313-335G>A p.(=) - - - -
SDHA 00001115 XM_005248331.1 0000020889 ./. - - c.442G>A p.(Ala148Thr) - - - -
SDHA 00001117 XR_241710.1 0000020889 ./. - - n.575G>A - - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000228365; RCV000287726; RCV000345164; RCV000383376; RCV000572868; RCV003475076;
Chromosome 5:225663..225663
Allele frequencies from ESP 0.00023
Allele frequencies from ExAC 0.00003
ClinVar Allele ID 239806
Disease database name and identifier MONDO:MONDO:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162|MONDO:MONDO:0100294, MedGen:C5700310, OMIM:252011, Orphanet:3208|MONDO:MONDO:0013602, MedGen:C3279992, OMIM:614165, Orphanet:29072|MONDO:MONDO:0017366, MedGen:C1708353, Orphanet:29072|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0013339, MedGen:C3150898, OMIM:613642, Orphanet:154
ClinVar preferred disease name Hereditary cancer-predisposing syndrome|Mitochondrial complex II deficiency, nuclear type 1|Paragangliomas 5|Hereditary pheochromocytoma-paraganglioma|Leigh syndrome|Dilated cardiomyopathy 1GG
HGVS variant names NC 000005.9:g.225663G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(5)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA3172820
Gene symbol:Gene id. SDHA:6389
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 375576259
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001895502;
Chromosome 5:225663..225663
ClinVar Allele ID 1496620
Disease database name and identifier MONDO:MONDO:0013602, MedGen:C3279992, OMIM:614165, Orphanet:29072|MONDO:MONDO:0100294, MedGen:C5700310, OMIM:252011, Orphanet:3208
ClinVar preferred disease name Paragangliomas 5|Mitochondrial complex II deficiency, nuclear type 1
HGVS variant names NC 000005.9:g.225663G>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SDHA:6389
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 375576259
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