Variant #0001015799 (NC_000019.9:g.42777457C>T, NM_015125.3:c.-11400C>T (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.42777457C>T
DNA change (hg38) -
Published as CIC(NM_001386298.1):c.1522C>T (p.R508*)
ISCN -
DB-ID CIC_000137
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +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     
CIC NM_001386298.1 +/. - c.1522C>T r.(?) p.(Arg508*)
CIC NM_015125.3 +/. - c.-11400C>T r.(?) p.(=)


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