Variant #0000270257 (NC_000001.10:g.16349137G>A, NM_004070.3:c.23G>A (CLCNKA))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.16349137G>A
DNA change (hg38) g.16022642G>A
Published as CLCNKA(NM_004070.4):c.23G>A (p.R8H)
ISCN -
DB-ID CLCNKA_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) 0.01581 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCNKA NM_004070.3 -/. - c.23G>A r.(?) p.(Arg8His)
HSPB7 NM_014424.4 -/. - c.-4679C>T r.(?) p.(=)


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