View genomic variant #0000001525

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.19373478C>G
Published as -
GERP -4.830
Segregation -
DB-ID PDHA1_000009 See all 2 reported entries
MSCV MSCV_0001525
dbSNP ID rs137853254
Frequency -
Sources ; clinvar; ensembl;
Reference 12379317;8199595
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
PDHA1 00000247 NM_000284.3 0000001525 +/+ - 7/11 c.615C>G p.(Phe205Leu) possibly_damaging(0.463) missense_variant - deleterious(0)
PDHA1 00000245 NM_001173454.1 0000001525 +/+ - 8/12 c.729C>G p.(Phe243Leu) possibly_damaging(0.586) missense_variant - deleterious(0)
PDHA1 00000246 NM_001173455.1 0000001525 +/+ - 7/11 c.636C>G p.(Phe212Leu) possibly_damaging(0.463) missense_variant - deleterious(0)
PDHA1 00000248 NM_001173456.1 0000001525 +/+ - 6/10 c.522C>G p.(Phe174Leu) benign(0.297) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000011629;
Chromosome X:19373478..19373478
ClinVar Allele ID 25921
Disease database name and identifier MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243
ClinVar preferred disease name Pyruvate dehydrogenase E1-alpha deficiency
HGVS variant names NC 000023.10:g.19373478C>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA121217|OMIM:300502.0012|UniProtKB:P08559#VAR 004954
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 137853254
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003093734;
Chromosome X:19373478..19373478
ClinVar Allele ID 1894127
Disease database name and identifier MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243
ClinVar preferred disease name Pyruvate dehydrogenase E1-alpha deficiency
HGVS variant names NC 000023.10:g.19373478C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
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