Variant #0000616867 (NC_000017.10:g.7750208_7750216dup, NM_001080424.1:c.783_791dup (KDM6B))

Chromosome 17
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.7750208_7750216dup
DNA change (hg38) g.7846890_7846898dup
Published as KDM6B(NM_001080424.1):c.752_753insACCACCACC (p.(Leu251_Pro252insProProPro)), KDM6B(NM_001080424.2):c.783_791dupACCACCACC (p.P262_P264dup)
ISCN -
DB-ID KDM6B_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_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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDM6B NM_001080424.1 -?/. - c.783_791dup r.(?) p.(Pro262_Pro264dup)


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