Variant #0000611122 (NC_000007.13:g.4825086_4825089dup, NC_000007.13(NM_014855.2):c.969+3_969+6dup (AP5Z1))

Chromosome 7
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.4825086_4825089dup
DNA change (hg38) g.4785455_4785458dup
Published as AP5Z1(NM_014855.3):c.969_969+1insGTAA
ISCN -
DB-ID AP5Z1_000060
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP5Z1 NM_014855.2 ?/. - c.969+3_969+6dup r.spl? p.?


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