Variant #0001067168 (NC_000019.9:g.36211117_36211125del, NM_014727.1:c.868_876del (KMT2B))

Chromosome 19
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.36211117_36211125del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr19_008920
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB32 NM_014383.1 -?/. - c.*3463_*3471del r.(=) p.(=)
KMT2B NM_014727.1 -?/. - c.868_876del r.(?) p.(Gly292_Gly294del)


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