Variant #0001015785 (NC_000019.9:g.36227600C>T, NM_014727.1:c.7169C>T (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.36227600C>T
DNA change (hg38) -
Published as KMT2B(NM_014727.3):c.7169C>T (p.S2390L)
ISCN -
DB-ID IGFLR1_000018
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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 -?/. - c.7169C>T r.(?) p.(Ser2390Leu)
IGFLR1 NM_024660.2 -?/. - c.*2581G>A r.(=) p.(=)
U2AF1L4 NM_144987.2 -?/. - c.*5899G>A r.(=) p.(=)


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