Variant #0000926899 (NC_000019.9:g.42796850_42796851insTCCTGCACCCAC, NM_015125.3:c.3308_3309insTCCTGCACCCAC (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.42796850_42796851insTCCTGCACCCAC
DNA change (hg38) -
Published as CIC(NM_015125.5):c.3308_3309insTCCTGCACCCAC (p.P1100_T1103dup)
ISCN -
DB-ID CIC_000104
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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +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.6035_6036insTCCTGCACCCAC r.(?) p.(Pro2009_Thr2012dup)
PAFAH1B3 NM_002573.3 ?/. - c.*4390_*4391insAGTGGGTGCAGG r.(=) p.(=)
CIC NM_015125.3 ?/. - c.3308_3309insTCCTGCACCCAC r.(?) p.(Pro1100_Thr1103dup)
PRR19 NM_199285.2 ?/. - c.-9812_-9811insTCCTGCACCCAC r.(?) p.(=)


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