Variant #0000567005 (NC_000019.9:g.36227707G>A, NM_014727.1:c.7276G>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.36227707G>A
DNA change (hg38) g.35736806G>A
Published as KMT2B(NM_014727.2):c.7276G>A (p.V2426I)
ISCN -
DB-ID IGFLR1_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) 0 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 ?/. - c.7276G>A r.(?) p.(Val2426Ile)
IGFLR1 NM_024660.2 ?/. - c.*2474C>T r.(=) p.(=)
U2AF1L4 NM_144987.2 ?/. - c.*5792C>T r.(=) p.(=)


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