Variant #0000621479 (NC_000005.9:g.137520280C>T, NM_005733.2:c.1598C>T (KIF20A))

Chromosome 5
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.137520280C>T
DNA change (hg38) g.138184591C>T
Published as KIF20A(NM_005733.3):c.1598C>T (p.P533L)
ISCN -
DB-ID CDC23_000008
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 2019-12-06 12:43:26 +01:00 (CET)
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     
CDC23 NM_004661.3 ?/. - c.*4387G>A r.(=) p.(=)
KIF20A NM_005733.2 ?/. - c.1598C>T r.(?) p.(Pro533Leu)


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