Variant #0000325502 (NC_000017.10:g.56056636_56056644del, NM_007146.2:c.1038_1046del (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.56056636_56056644del
DNA change (hg38) g.57979275_57979283del
Published as VEZF1(NM_007146.2):c.1038_1046del (p.(Gln350_Gln352del))
ISCN -
DB-ID VEZF1_000002
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VEZF1 NM_007146.2 ?/. - c.1038_1046del r.(?) p.(Gln352_Gln354del)


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