Variant #0000967116 (NC_000013.10:g.100622683_100622703del, NM_033132.3:c.1242_1262del (ZIC5))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100622683_100622703del
DNA change (hg38) -
Published as ZIC5(NM_033132.5):c.1170_1190delGCCGCCGCCGCCGCCGCCGCC (p.P394_P400del)
ISCN -
DB-ID ZIC5_000007
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
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.1242_1262del r.(?) p.(Pro418_Pro424del)


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