Variant #0000866233 (NC_000019.9:g.50412206T>C, NM_001193646.1:c.-20571T>C (ATF5))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50412206T>C
DNA change (hg38) -
Published as NUP62(NM_016553.4):c.859A>G (p.T287A)
ISCN -
DB-ID ATF5_000019
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) 5.0E-5 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATF5 NM_001193646.1 -?/. - c.-20571T>C r.(?) p.(=)
IL4I1 NM_001258017.1 -?/. - c.-227-4628A>G r.(=) p.(=)
NUP62 NM_153719.3 -?/. - c.859A>G r.(?) p.(Thr287Ala)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.