Variant #0000862981 (NC_000012.11:g.45822904_45822905del, NM_001025356.2:c.2543_2544del (ANO6))

Chromosome 12
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.45822904_45822905del
DNA change (hg38) -
Published as ANO6(NM_001204803.1):c.2606_2607delTG (p.V869Efs*32)
ISCN -
DB-ID ANO6_000007
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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     
ANO6 NM_001025356.2 +/. - c.2543_2544del r.(?) p.(Val848Glufs*32)


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