View genomic variant #0000001534

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type del
DNA change (genomic) (Relative to hg19 / GRCh37) g.19377071_19377073del
Published as -
GERP -
Segregation -
DB-ID PDHA1_000006 See all 2 reported entries
MSCV MSCV_0001534
dbSNP ID -
Frequency -
Sources ;
Reference -
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 0000001534 ./. - - c.937_939del p.(Lys313del) - - - -
PDHA1 00000245 NM_001173454.1 0000001534 ./. - - c.1051_1053del p.(Lys351del) - - - -
PDHA1 00000246 NM_001173455.1 0000001534 ./. - - c.958_960del p.(Lys320del) - - - -
PDHA1 00000248 NM_001173456.1 0000001534 ./. - - c.844_846del p.(Lys282del) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000196049; RCV001224932;
Chromosome X:19377070..19377071
ClinVar Allele ID 212016
Disease database name and identifier MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243|MedGen:CN517202
ClinVar preferred disease name Pyruvate dehydrogenase E1-alpha deficiency|not provided
HGVS variant names NC 000023.10:g.19377071 19377074dup
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA320449
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 137853251
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000011621;
Chromosome X:19377071..19377073
ClinVar Allele ID 25913
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.19377072 19377074del
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA121206|OMIM:300502.0004
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001822|inframe deletion
Allele origin germline
dbSNP ID 137853251
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