Variant #0000539855 (NC_000010.10:g.31810782A>C, NM_030751.5:c.2519A>C (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.31810782A>C
DNA change (hg38) g.31521854A>C
Published as ZEB1(NM_001323638.1):c.1865A>C (p.Q622P), ZEB1(NM_030751.6):c.2519A>C (p.Q840P)
ISCN -
DB-ID ZEB1_000046 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) 0.00758 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.2522A>C r.(?) p.(Gln841Pro)
ZEB1 NM_030751.5 ?/. - c.2519A>C r.(?) p.(Gln840Pro)


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