Variant #0000357611 (NC_000023.10:g.15349518T>A, PIGA(NM_002641.3):c.535A>T)

Individual ID 00155009
Chromosome X
Allele Maternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.15349518T>A
DNA change (hg38) g.15331396T>A
Published as -
ISCN -
DB-ID PIGA_000052 See all 2 reported entries
Variant remarks -
Reference PubMed: Joshi et al. 2016
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Philippe Campeau
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Philippe Campeau
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGA NM_002641.3 +?/. - c.535A>T r.(?) p.(Asn179Tyr)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000155872 DNA SEQ-NG - WES - 1 Philippe Campeau