Variant #0000560738 (NC_000017.10:g.27068158C>T, NM_178170.2:c.1795C>T (NEK8))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27068158C>T
DNA change (hg38) g.28741140C>T
Published as NEK8(NM_178170.3):c.1795C>T (p.R599*)
ISCN -
DB-ID NEK8_000014 See all 3 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) 6.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAF4 NM_004295.3 +/. - c.-2973C>T r.(?) p.(=)
NEK8 NM_178170.2 +/. - c.1795C>T r.(?) p.(Arg599Ter)


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