Variant #0000677233 (NC_000004.11:g.170483284A>G, NC_000004.11(NM_001199397.1):c.1080+4T>C (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.170483284A>G
DNA change (hg38) -
Published as NEK1(NM_001199397.1):c.1080+4T>C (p.?), NEK1(NM_001199397.2):c.1080+4T>C, NEK1(NM_001199397.3):c.1080+4T>C
ISCN -
DB-ID NEK1_000039 See all 4 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) 7.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +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.1080+4T>C r.spl? p.?


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