Variant #0000126698 (NC_000011.9:g.22247558T>G, ANO5(NM_213599.2):c.323T>G)

Individual ID 00078831
Chromosome 11
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.22247558T>G
DNA change (hg38) g.22226012T>G
Published as -
ISCN -
DB-ID ANO5_000050 See all 2 reported entries
Variant remarks -
Reference PubMed: Sarkozy 2012
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANO5 NM_213599.2 +/. 6 c.323T>G r.(?) p.(Leu108Arg)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000079019 DNA SEQ - - ANO5 2 Johan den Dunnen