Variant #0000618614 (NC_000022.10:g.41634093_41634100dup, NM_138481.1:c.981_988dup (CHADL))

Chromosome 22
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.41634093_41634100dup
DNA change (hg38) g.41238089_41238096dup
Published as CHADL(NM_138481.1):c.988_989insGGCGCGCG (p.(Val330GlyfsTer106))
ISCN -
DB-ID CHADL_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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-17 13:45:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
L3MBTL2 NM_031488.4 -?/. - c.*7838_*7845dup r.(=) p.(=)
CHADL NM_138481.1 -?/. - c.981_988dup r.(?) p.(Val330GlyfsTer106)


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