Variant #0000618003 (NC_000020.10:g.21186163_21186164insA, NM_018474.4:c.1387_1388insA (KIZ))

Chromosome 20
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.21186163_21186164insA
DNA change (hg38) g.21205525_21205526insA
Published as PLK1S1(NM_001163022.1):c.1077_1078insA (p.(His360ThrfsTer212))
ISCN -
DB-ID KIZ_000026
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 15:13:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIZ NM_018474.4 -?/. - c.1387_1388insA r.(?) p.(Ala463AspfsTer14)


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