Variant #0000894935 (NC_000019.9:g.36227852G>A, NM_014727.1:c.7337G>A (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.36227852G>A
DNA change (hg38) -
Published as KMT2B(NM_014727.3):c.7337G>A (p.R2446Q)
ISCN -
DB-ID IGFLR1_000014
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) 0 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 ?/. - c.7337G>A r.(?) p.(Arg2446Gln)
IGFLR1 NM_024660.2 ?/. - c.*2329C>T r.(=) p.(=)
U2AF1L4 NM_144987.2 ?/. - c.*5647C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.