Variant #0000321479 (NC_000010.10:g.31816024_31816026del, NM_030751.5:c.3207_3209del (ZEB1))

Chromosome 10
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.31816024_31816026del
DNA change (hg38) g.31527096_31527098del
Published as ZEB1(NM_001128128.2):c.3145_3147del (p.(Glu1049del))
ISCN -
DB-ID ZEB1_000009
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZEB1 NM_001174096.1 -?/. - c.3210_3212del r.(?) p.(Glu1072del)
ZEB1 NM_030751.5 -?/. - c.3207_3209del r.(?) p.(Glu1071del)


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