Variant #0000296653 (NC_000019.9:g.50412417G>A, NM_001193646.1:c.-20360G>A (ATF5))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50412417G>A
DNA change (hg38) g.49909160G>A
Published as IL4I1(NM_001258018.2):c.-285-4839C>T, NUP62(NM_016553.5):c.648C>T (p.S216=)
ISCN -
DB-ID IL4I1_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) 0.79147 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATF5 NM_001193646.1 -/. - c.-20360G>A r.(?) p.(=)
IL4I1 NM_001258017.1 -/. - c.-227-4839C>T r.(=) p.(=)
NUP62 NM_153719.3 -/. - c.648C>T r.(?) p.(Ser216=)


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