Variant #0000692814 (NC_000019.9:g.42798375_42798377dup, NM_015125.3:c.4246_4248dup (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.42798375_42798377dup
DNA change (hg38) -
Published as CIC(NM_015125.5):c.4246_4248dupAGA (p.R1417dup)
ISCN -
DB-ID CIC_000064
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAFAH1B3 NM_002573.3 ?/. - c.*2856_*2858dup r.(=) p.(=)
CIC NM_015125.3 ?/. - c.4246_4248dup r.(?) p.(Arg1417dup)
PRR19 NM_199285.2 ?/. - c.-8287_-8285dup r.(?) p.(=)


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