Variant #0000658544 (NC_000019.9:g.36211138C>T, NM_014727.1:c.889C>T (KMT2B))

Chromosome 19
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.36211138C>T
DNA change (hg38) g.35720236C>T
Published as KMT2B(NM_014727.2):c.889C>T (p.R297*)
ISCN -
DB-ID ZBTB32_000021
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-15 17:04:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB32 NM_014383.1 +/. - c.*3484C>T r.(=) p.(=)
KMT2B NM_014727.1 +/. - c.889C>T r.(?) p.(Arg297Ter)


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