Variant #0000504068 (NC_000001.10:g.16375584del, NC_000001.10(NM_000085.4):c.656-31del (CLCNKB))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.16375584del
DNA change (hg38) g.16049089del
Published as CLCNKB(NM_001165945.2):c.118del (p.(Arg40GlyfsTer4)), CLCNKB(NM_001165945.2):c.118delA (p.R40Gfs*4)
ISCN -
DB-ID CLCNKB_000067 See all 2 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) 0.00056 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCNKB NM_000085.4 +?/. - c.656-31del r.(=) p.(=)


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