Variant #0000681386 (NC_000019.9:g.36237625T>G, NM_014727.1:c.*8167T>G (KMT2B))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36237625T>G
DNA change (hg38) -
Published as PSENEN(NM_172341.4):c.183T>G (p.A61=)
ISCN -
DB-ID IGFLR1_000010
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 -?/. - c.*8167T>G r.(=) p.(=)
LIN37 NM_019104.2 -?/. - c.-2001T>G r.(?) p.(=)
IGFLR1 NM_024660.2 -?/. - c.-4372A>C r.(?) p.(=)
U2AF1L4 NM_144987.2 -?/. - c.-1333A>C r.(?) p.(=)
PSENEN NM_172341.1 -?/. - c.183T>G r.(?) p.(Ala61=)


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