Variant #0000690717 (NC_000010.10:g.31812927A>C, NM_030751.5:c.2668A>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.31812927A>C
DNA change (hg38) -
Published as ZEB1(NM_001323638.1):c.2014A>C (p.T672P)
ISCN -
DB-ID ZEB1_000058
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) 0.00013 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 2020-09-15 15:50:26 +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.2671A>C r.(?) p.(Thr891Pro)
ZEB1 NM_030751.5 ?/. - c.2668A>C r.(?) p.(Thr890Pro)


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