Variant #0000563375 (NC_000017.10:g.7755291C>T, NM_001080424.1:c.4188C>T (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.7755291C>T
DNA change (hg38) g.7851973C>T
Published as KDM6B(NM_001080424.2):c.4188C>T (p.F1396=)
ISCN -
DB-ID CYB5D1_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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-11 15:59:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDM6B NM_001080424.1 -?/. - c.4188C>T r.(?) p.(Phe1396=)
LSMD1 NM_032356.3 -?/. - c.*4758G>A r.(=) p.(=)
CYB5D1 NM_144607.4 -?/. - c.-6162C>T r.(?) p.(=)
TMEM88 NM_203411.1 -?/. - c.-3102C>T r.(?) p.(=)


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