Variant #0000948287 (NC_000004.11:g.170506525C>T, NM_001199397.1:c.782G>A (NEK1))

Chromosome 4
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.170506525C>T
DNA change (hg38) -
Published as NEK1(NM_001199397.1):c.782G>A (p.R261H, p.(Arg261His)), NEK1(NM_001374418.1):c.782G>A (p.R261H), NEK1(NM_012224.4):c.782G>A (p.R261H)
ISCN -
DB-ID NEK1_000024 See all 6 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) 0.00236 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 2023-11-27 17:35:39 +01:00 (CET)
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.782G>A r.(?) p.(Arg261His)


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