Variant #0000532081 (NC_000007.13:g.44805819_44805820del, NM_031449.3:c.2299_2300del (ZMIZ2))

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.44805819_44805820del
DNA change (hg38) g.44766220_44766221del
Published as ZMIZ2(NM_031449.3):c.2299_2300del (p.(Ser767HisfsTer6))
ISCN -
DB-ID ZMIZ2_000005
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-22 15:55:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZMIZ2 NM_031449.3 -?/. - c.2299_2300del r.(?) p.(Ser767HisfsTer6)


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