Variant #0000303001 (NC_000004.11:g.170429402T>C, NM_001199397.1:c.1830A>G (NEK1))

Chromosome 4
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.170429402T>C
DNA change (hg38) g.169508251T>C
Published as NEK1(NM_001199397.1):c.1830A>G (p.E610=), NEK1(NM_001199397.3):c.1830A>G (p.E610=)
ISCN -
DB-ID NEK1_000017 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) 0.04755 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEK1 NM_001199397.1 -/. - c.1830A>G r.(?) p.(Glu610=)


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