Variant #0000524279 (NC_000005.9:g.137520248G>A, NM_005733.2:c.1566G>A (KIF20A))

Chromosome 5
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.137520248G>A
DNA change (hg38) g.138184559G>A
Published as KIF20A(NM_005733.3):c.1566G>A (p.S522=)
ISCN -
DB-ID CDC23_000004
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) 0.00014 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 2020-06-17 15:16:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDC23 NM_004661.3 -?/. - c.*4419C>T r.(=) p.(=)
KIF20A NM_005733.2 -?/. - c.1566G>A r.(?) p.(Ser522=)


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