Variant #0000566960 (NC_000019.9:g.36210765C>A, NM_014727.1:c.516C>A (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.36210765C>A
DNA change (hg38) g.35719863C>A
Published as KMT2B(NM_014727.2):c.516C>A (p.T172=)
ISCN -
DB-ID ZBTB32_000003
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) 2.0E-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 2024-04-19 20:27:30 +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.*3111C>A r.(=) p.(=)
KMT2B NM_014727.1 -?/. - c.516C>A r.(?) p.(Thr172=)


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