Variant #0000911844 (NC_000003.11:g.147128227G>C, NM_003412.3:c.328G>C (ZIC1))

Chromosome 3
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.147128227G>C
DNA change (hg38) -
Published as ZIC1(NM_003412.3):c.328G>C (p.A110P), ZIC1(NM_003412.4):c.328G>C (p.A110P)
ISCN -
DB-ID ZIC1_000006 See all 2 reported entries
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) 0.0004 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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     
ZIC4 NM_001168378.1 -?/. - c.-6342C>G r.(?) p.(=)
ZIC1 NM_003412.3 -?/. - c.328G>C r.(?) p.(Ala110Pro)


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