Variant #0000977450 (NC_000007.13:g.104752851_104752859del, NM_182931.3:c.4648_4656del (MLL5))

Chromosome 7
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.104752851_104752859del
DNA change (hg38) -
Published as KMT2E(NM_182931.3):c.4648_4656del (p.(Pro1550_Pro1552del)), KMT2E(NM_182931.3):c.4648_4656delCCACCTCCT (p.P1550_P1552del)
ISCN -
DB-ID MLL5_000098 See all 2 reported entries
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLL5 NM_182931.3 -?/. - c.4648_4656del r.(?) p.(Pro1550_Pro1552del)


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