Variant #0000979020 (NC_000010.10:g.31749984_31749989del, NM_030751.5:c.77_82del (ZEB1))

Chromosome 10
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.31749984_31749989del
DNA change (hg38) -
Published as ZEB1(NM_001128128.2):c.26_31delTGGTAG (p.V9_V10del), ZEB1(NM_001174096.2):c.77_82del (p.(Val26_Val27del))
ISCN -
DB-ID ZEB1_000053 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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZEB1 NM_001174096.1 ?/. - c.77_82del r.(?) p.(Val26_Val27del)
ZEB1 NM_030751.5 ?/. - c.77_82del r.(?) p.(Val26_Val27del)


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