Variant #0000967166 (NC_000013.10:g.20641513del, NM_197968.2:c.3436del (ZMYM2))

Chromosome 13
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.20641513del
DNA change (hg38) -
Published as ZMYM2(NM_001353162.1):c.3436delT (p.C1146Afs*30), ZMYM2(NM_003453.4):c.3436delT (p.C1146Afs*30)
ISCN -
DB-ID ZMYM2_000048
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2024-02-26 20:06:56 +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     
ZMYM2 NM_197968.2 ?/. - c.3436del r.(?) p.(Cys1146Alafs*30)


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