Variant #0000724373 (NC_000013.10:g.20625714_20625717del, NM_197968.2:c.2434_2437del (ZMYM2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.20625714_20625717del
DNA change (hg38) -
Published as ZMYM2(NM_003453.6):c.2434_2437delAAAG (p.K812Dfs*18)
ISCN -
DB-ID ZMYM2_000001 See all 3 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZMYM2 NM_197968.2 +?/. - c.2434_2437del r.(?) p.(Lys812AspfsTer18)


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