Variant #0000560741 (NC_000017.10:g.27068531C>G, NM_178170.2:c.1992C>G (NEK8))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.27068531C>G
DNA change (hg38) g.28741513C>G
Published as NEK8(NM_178170.3):c.1992C>G (p.H664Q)
ISCN -
DB-ID NEK8_000016
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAF4 NM_004295.3 ?/. - c.-2600C>G r.(?) p.(=)
NEK8 NM_178170.2 ?/. - c.1992C>G r.(?) p.(His664Gln)


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