Variant #0000608375 (NC_000003.11:g.147127924T>C, NM_003412.3:c.25T>C (ZIC1))

Chromosome 3
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.147127924T>C
DNA change (hg38) g.147410137T>C
Published as ZIC1(NM_003412.3):c.25T>C (p.Y9H)
ISCN -
DB-ID ZIC1_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +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     
ZIC4 NM_001168378.1 ?/. - c.-6039A>G r.(?) p.(=)
ZIC1 NM_003412.3 ?/. - c.25T>C r.(?) p.(Tyr9His)


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