Variant #0001004827 (NC_000019.9:g.42797110G>A, NM_015125.3:c.3472G>A (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.42797110G>A
DNA change (hg38) -
Published as CIC(NM_001379480.1):c.6197-1G>A (p.(Gly1158Ser))
ISCN -
DB-ID CIC_000132
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) 1.0E-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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CIC NM_001386298.1 ?/. - c.6199G>A r.(?) p.(Gly2067Ser)
PAFAH1B3 NM_002573.3 ?/. - c.*4120C>T r.(=) p.(=)
CIC NM_015125.3 ?/. - c.3472G>A r.(?) p.(Gly1158Ser)
PRR19 NM_199285.2 ?/. - c.-9552G>A r.(?) p.(=)


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