Variant #0000522214 (NC_000004.11:g.184174909G>T, NM_001111319.1:c.*65800C>A (CLDN22))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.184174909G>T
DNA change (hg38) g.183253756G>T
Published as WWC2(NM_024949.5):c.954-1G>T (p.?)
ISCN -
DB-ID CLDN22_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 16:44:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLDN22 NM_001111319.1 -?/. - c.*65800C>A r.(=) p.(=)
WWC2 NM_024949.5 -?/. - c.954-1G>T r.spl? p.?


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