Variant #0000924083 (NC_000004.11:g.170508758_170508764del, NM_001199397.1:c.554_560del (NEK1))

Chromosome 4
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.170508758_170508764del
DNA change (hg38) -
Published as NEK1(NM_001374418.1):c.554_560delACATTTG (p.D185Gfs*22)
ISCN -
DB-ID NEK1_000090
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEK1 NM_001199397.1 +?/. - c.554_560del r.(?) p.(Asp185Glyfs*22)


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