Variant #0001067212 (NC_000019.9:g.42799295_42799296insGGCG, NM_015125.3:c.4779_4780insGGCG (CIC))

Chromosome 19
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.42799295_42799296insGGCG
DNA change (hg38) -
Published as CIC(NM_001386298.1):c.7506_7507insGGCG (p.(Pro2503Glyfs*21))
ISCN -
DB-ID CIC_000161
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +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.7506_7507insGGCG r.(?) p.(Pro2503Glyfs*21)
PAFAH1B3 NM_002573.3 ?/. - c.*1935_*1936insGCCC r.(=) p.(=)
CIC NM_015125.3 ?/. - c.4779_4780insGGCG r.(?) p.(Pro1594Glyfs*21)
PRR19 NM_199285.2 ?/. - c.-7367_-7366insGGCG r.(?) p.(=)


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