Variant #0000530064 (NC_000007.13:g.100366248_100366250del, NM_003386.1:c.5057_5059del (ZAN))

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.100366248_100366250del
DNA change (hg38) g.100768625_100768627del
Published as ZAN(NM_003386.1):c.5048_5050del (p.(Asn1685del))
ISCN -
DB-ID ZAN_000011
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 11:09:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZAN NM_003386.1 ?/. - c.5057_5059del r.(?) p.(Asn1686del)


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