Variant #0001004662 (NC_000019.9:g.36228099G>T, NM_014727.1:c.7485G>T (KMT2B))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36228099G>T
DNA change (hg38) -
Published as KMT2B(NM_014727.1):c.7485G>T (p.(Gln2495His))
ISCN -
DB-ID IGFLR1_000017
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 ?/. - c.7485G>T r.(?) p.(Gln2495His)
IGFLR1 NM_024660.2 ?/. - c.*2082C>A r.(=) p.(=)
U2AF1L4 NM_144987.2 ?/. - c.*5400C>A r.(=) p.(=)


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