Variant #0000854796 (NC_000017.10:g.27066227C>T, NC_000017.10(NM_178170.2):c.1417+8C>T (NEK8))

Chromosome 17
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.27066227C>T
DNA change (hg38) -
Published as NEK8(NM_178170.3):c.1417+8C>T
ISCN -
DB-ID NEK8_000037
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) 2.0E-5 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 2022-05-09 15:47:41 +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     
TRAF4 NM_004295.3 -?/. - c.-4904C>T r.(?) p.(=)
NEK8 NM_178170.2 -?/. - c.1417+8C>T r.(=) p.(=)


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