Variant #0000692742 (NC_000019.9:g.33464469G>C, NM_032816.3:c.-1689C>G (CEP89))

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.33464469G>C
DNA change (hg38) -
Published as FAAP24(NM_152266.4):c.243+1G>C
ISCN -
DB-ID C19orf40_000004
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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP89 NM_032816.3 ?/. - c.-1689C>G r.(?) p.(=)
C19orf40 NM_152266.3 ?/. - c.243+1G>C r.spl? p.?


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