View genomic variant #0000001528

Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.19373593A>C
Published as -
GERP 5.760
Segregation -
DB-ID PDHA1_000012
MSCV MSCV_0001528
dbSNP ID NA
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 0000001528 ./. - 7/11 c.730A>C p.(Lys244Gln) possibly_damaging(0.489) missense_variant - tolerated(0.09)
PDHA1 00000245 NM_001173454.1 0000001528 ./. - 8/12 c.844A>C p.(Lys282Gln) possibly_damaging(0.585) missense_variant - deleterious(0.05)
PDHA1 00000246 NM_001173455.1 0000001528 ./. - 7/11 c.751A>C p.(Lys251Gln) possibly_damaging(0.489) missense_variant - tolerated(0.1)
PDHA1 00000248 NM_001173456.1 0000001528 ./. - 6/10 c.637A>C p.(Lys213Gln) probably_damaging(0.911) missense_variant - tolerated(0.13)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003197952;
Chromosome X:19373593..19373593
ClinVar Allele ID 2445912
Disease database name and identifier MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name Inborn genetic diseases
HGVS variant names NC 000023.10:g.19373593A>G
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. PDHA1:5160
Molecular consequence SO:0001583|missense 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