Variant #0001042994 (NC_000019.9:g.42796862C>T, NM_015125.3:c.3320C>T (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.42796862C>T
DNA change (hg38) -
Published as CIC(NM_015125.5):c.3320C>T (p.P1107L)
ISCN -
DB-ID CIC_000141
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) 2.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CIC NM_001386298.1 -?/. - c.6047C>T r.(?) p.(Pro2016Leu)
PAFAH1B3 NM_002573.3 -?/. - c.*4368G>A r.(=) p.(=)
CIC NM_015125.3 -?/. - c.3320C>T r.(?) p.(Pro1107Leu)
PRR19 NM_199285.2 -?/. - c.-9800C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.