Variant #0001004831 (NC_000019.9:g.42799293_42799294insCG, NM_015125.3:c.4777_4778insCG (CIC))

Chromosome 19
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.42799293_42799294insCG
DNA change (hg38) -
Published as CIC(NM_001304815.1):c.7504_7505insCG (p.Q2502Pfs*28), CIC(NM_015125.3):c.4777_4778insCG (p.(Gln1593fs))
ISCN -
DB-ID CIC_000065 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) 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 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     
PAFAH1B3 NM_002573.3 -?/. - c.*1936_*1937insCG r.(=) p.(=)
CIC NM_015125.3 -?/. - c.4777_4778insCG r.(?) p.(Gln1593ProfsTer28)
PRR19 NM_199285.2 -?/. - c.-7369_-7368insCG r.(?) p.(=)


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