Variant #0000727400 (NC_000019.9:g.42797904C>T, NM_015125.3:c.3956C>T (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.42797904C>T
DNA change (hg38) -
Published as CIC(NM_015125.5):c.3956C>T (p.P1319L)
ISCN -
DB-ID CIC_000082
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 2021-02-08 18:36:18 +01:00 (CET)
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.*3326G>A r.(=) p.(=)
CIC NM_015125.3 ?/. - c.3956C>T r.(?) p.(Pro1319Leu)
PRR19 NM_199285.2 ?/. - c.-8758C>T r.(?) p.(=)


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