Variant #0000692743 (NC_000019.9:g.33464993G>A, NM_032816.3:c.-2213C>T (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.33464993G>A
DNA change (hg38) -
Published as FAAP24(NM_152266.5):c.271G>A (p.V91I)
ISCN -
DB-ID C19orf40_000005
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP89 NM_032816.3 ?/. - c.-2213C>T r.(?) p.(=)
RHPN2 NM_033103.4 ?/. - c.*5909C>T r.(=) p.(=)
C19orf40 NM_152266.3 ?/. - c.271G>A r.(?) p.(Val91Ile)


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