Variant #0000560742 (NC_000017.10:g.27068978G>A, NM_178170.2:c.2052G>A (NEK8))

Chromosome 17
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.27068978G>A
DNA change (hg38) g.28741960G>A
Published as NEK8(NM_178170.3):c.2052G>A (p.S684=)
ISCN -
DB-ID NEK8_000017
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) 0.00763 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 2020-07-13 11:12:40 +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.-2153G>A r.(?) p.(=)
NEK8 NM_178170.2 -/. - c.2052G>A r.(?) p.(Ser684=)


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