Variant #0001042875 (NC_000019.9:g.36228809_36228813del, NM_014727.1:c.7708_7712del (KMT2B))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36228809_36228813del
DNA change (hg38) -
Published as KMT2B(NM_014727.3):c.7708_7712del (p.(Lys2570Aspfs*21))
ISCN -
DB-ID IGFLR1_000019
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.7708_7712del r.(?) p.(Lys2570Aspfs*21)
IGFLR1 NM_024660.2 +?/. - c.*1368_*1372del r.(=) p.(=)
U2AF1L4 NM_144987.2 +?/. - c.*4686_*4690del r.(=) p.(=)


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