Variant #0000604975 (NC_000001.10:g.16376380_16376383dup, NM_000085.4:c.937_940dup (CLCNKB))

Chromosome 1
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.16376380_16376383dup
DNA change (hg38) g.16049885_16049888dup
Published as CLCNKB(NM_000085.4):c.937_940dupAATA (p.R314Kfs*2)
ISCN -
DB-ID CLCNKB_000073
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.937_940dup r.(?) p.(Arg314LysfsTer2)


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