Variant #0000808812 (NC_000019.9:g.33467575C>T, NM_032816.3:c.-4795G>A (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.33467575C>T
DNA change (hg38) -
Published as FAAP24(NM_152266.4):c.635C>T (p.T212M), FAAP24(NM_152266.5):c.635C>T (p.T212M)
ISCN -
DB-ID C19orf40_000006 See all 2 reported entries
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) 0.00237 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 2021-09-17 14:40:49 +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.-4795G>A r.(?) p.(=)
RHPN2 NM_033103.4 ?/. - c.*3327G>A r.(=) p.(=)
C19orf40 NM_152266.3 ?/. - c.635C>T r.(?) p.(Thr212Met)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.