Variant #0000623079 (NC_000014.8:g.100706149_100706162del, NM_003403.4:c.568_581del (YY1))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100706149_100706162del
DNA change (hg38) g.100239812_100239825del
Published as YY1(NM_003403.5):c.568_581delGCCGGCGCGGCGGG (p.A190Rfs*34)
ISCN -
DB-ID YY1_000009 See all 2 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YY1 NM_003403.4 +/. - c.568_581del r.(?) p.(Ala190ArgfsTer34)


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