View genomic variant #0000001524

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.19373476T>A
Published as -
GERP 5.760
Segregation -
DB-ID PDHA1_000014
MSCV MSCV_0001524
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 0000001524 ./. - 7/11 c.613T>A p.(Phe205Ile) possibly_damaging(0.811) missense_variant - deleterious(0)
PDHA1 00000245 NM_001173454.1 0000001524 ./. - 8/12 c.727T>A p.(Phe243Ile) possibly_damaging(0.876) missense_variant - deleterious(0)
PDHA1 00000246 NM_001173455.1 0000001524 ./. - 7/11 c.634T>A p.(Phe212Ile) possibly_damaging(0.811) missense_variant - deleterious(0)
PDHA1 00000248 NM_001173456.1 0000001524 ./. - 6/10 c.520T>A p.(Phe174Ile) possibly_damaging(0.678) missense_variant - deleterious(0)
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None