Variant #0000927825 (NC_000011.9:g.22296266C>T, NM_213599.2:c.2387C>T (ANO5))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.22296266C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ANO5_000053 See all 13 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs61910685
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00871 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-06-16 16:00:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANO5 NM_213599.2 ?/. - c.2387C>T r.(?) p.(Ser796Leu)


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