Variant #0000528150 (NC_000006.11:g.28212901_28212903del, NM_019110.3:c.1629_1631del (ZKSCAN4))

Chromosome 6
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.28212901_28212903del
DNA change (hg38) g.28245123_28245125del
Published as ZKSCAN4(NM_019110.3):c.1629_1631del (p.(Ser544del))
ISCN -
DB-ID ZKSCAN4_000002
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) 0.00095 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 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     
ZKSCAN4 NM_019110.3 -?/. - c.1629_1631del r.(?) p.(Ser544del)


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