Variant #0000889772 (NC_000011.9:g.22284590G>A, NC_000011.9(NM_213599.2):c.1898+1G>A (ANO5))

Chromosome 11
Allele Unknown
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.22284590G>A
DNA change (hg38) -
Published as ANO5(NM_001142649.1):c.1895+1G>A (p.?), ANO5(NM_001142649.2):c.1895+1G>A, ANO5(NM_213599.2):c.1898+1G>A, ANO5(NM_213599.3):c.1898+1G>A
ISCN -
DB-ID ANO5_000033 See all 59 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANO5 NM_213599.2 +/. - c.1898+1G>A r.spl? p.?


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