Variant #0000691453 (NC_000013.10:g.100622701_100622703dup, NM_033132.3:c.1260_1262dup (ZIC5))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100622701_100622703dup
DNA change (hg38) -
Published as ZIC5(NM_033132.4):c.1260_1262dupGCC (p.P424dup)
ISCN -
DB-ID ZIC5_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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZIC5 NM_033132.3 -/. - c.1260_1262dup r.(?) p.(Pro424dup)


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