Genomic variant #0000126655

Individual ID 00078761
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.22283777T>C
DNA change (hg38) g.22262231T>C
Published as -
ISCN -
DB-ID ANO5_000031 See all 10 reported entries
Variant remarks -
Reference PubMed: Hicks 2011
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00015 View details
Owner Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANO5 NM_213599.2 +/. 16 c.1733T>C r.(?) p.(Phe578Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000078949 DNA SEQ - - ANO5 2 Johan den Dunnen