Variant #0001056694 (NC_000019.9:g.42797805G>A, NM_015125.3:c.3857G>A (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.42797805G>A
DNA change (hg38) -
Published as CIC(NM_001386298.1):c.6584G>A (p.(Arg2195His))
ISCN -
DB-ID CIC_000155
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.6584G>A r.(?) p.(Arg2195His)
PAFAH1B3 NM_002573.3 -?/. - c.*3425C>T r.(=) p.(=)
CIC NM_015125.3 -?/. - c.3857G>A r.(?) p.(Arg1286His)
PRR19 NM_199285.2 -?/. - c.-8857G>A r.(?) p.(=)


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