Variant #0000290156 (NC_000017.10:g.7755271C>T, NM_001080424.1:c.4168C>T (KDM6B))

Chromosome 17
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.7755271C>T
DNA change (hg38) g.7851953C>T
Published as KDM6B(NM_001080424.2):c.4168C>T (p.H1390Y)
ISCN -
DB-ID KDM6B_000022
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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     
KDM6B NM_001080424.1 ?/. - c.4168C>T r.(?) p.(His1390Tyr)
LSMD1 NM_032356.3 ?/. - c.*4778G>A r.(=) p.(=)
CYB5D1 NM_144607.4 ?/. - c.-6182C>T r.(?) p.(=)
TMEM88 NM_203411.1 ?/. - c.-3122C>T r.(?) p.(=)


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