Variant #0001004635 (NC_000019.9:g.36212107C>G, NM_014727.1:c.1858C>G (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.36212107C>G
DNA change (hg38) -
Published as KMT2B(NM_014727.1):c.1858C>G (p.(Pro620Ala))
ISCN -
DB-ID ZBTB32_000051
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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB32 NM_014383.1 ?/. - c.*4453C>G r.(=) p.(=)
KMT2B NM_014727.1 ?/. - c.1858C>G r.(?) p.(Pro620Ala)


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