Variant #0001004814 (NC_000019.9:g.42776823C>G, NM_015125.3:c.-12034C>G (CIC))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42776823C>G
DNA change (hg38) -
Published as CIC(NM_001304815.1):c.888C>G (p.Y296*)
ISCN -
DB-ID CIC_000119
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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     
CIC NM_001386298.1 +/. - c.888C>G r.(?) p.(Tyr296*)
CIC NM_015125.3 +/. - c.-12034C>G r.(?) p.(=)


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