Variant #0000248713 (NC_000019.9:g.50411742A>G, NM_001193646.1:c.-21035A>G (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.50411742A>G
DNA change (hg38) g.49908485A>G
Published as IL4I1(NM_001258018.2):c.-285-4164T>C, NUP62(NM_016553.5):c.1323T>C (p.D441=)
ISCN -
DB-ID NUP62_000001
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) 0.94425 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.-21035A>G r.(?) p.(=)
IL4I1 NM_001258017.1 -/. - c.-227-4164T>C r.(=) p.(=)
NUP62 NM_153719.3 -/. - c.1323T>C r.(?) p.(Asp441=)


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