Variant #0000983386 (NC_000019.9:g.36213930C>T, NM_014727.1:c.2756C>T (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.36213930C>T
DNA change (hg38) -
Published as KMT2B(NM_014727.2):c.2756C>T (p.P919L), KMT2B(NM_014727.3):c.2756C>T (p.(Pro919Leu))
ISCN -
DB-ID KMT2B_000040 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 -?/. - c.2756C>T r.(?) p.(Pro919Leu)


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