Variant #0000325506 (NC_000017.10:g.56056642_56056644dup, NM_007146.2:c.1044_1046dup (VEZF1))

Chromosome 17
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.56056642_56056644dup
DNA change (hg38) g.57979281_57979283dup
Published as VEZF1(NM_007146.2):c.1032_1034dup (p.(Gln349dup))
ISCN -
DB-ID VEZF1_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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VEZF1 NM_007146.2 ?/. - c.1044_1046dup r.(?) p.(Gln354dup)


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