Variant #0001043119 (NC_000019.9:g.50411547G>A, NM_001193646.1:c.-21230G>A (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.50411547G>A
DNA change (hg38) -
Published as NUP62(NM_016553.4):c.1518C>T (p.C506=), NUP62(NM_016553.5):c.1518C>T (p.(Cys506=))
ISCN -
DB-ID IL4I1_000001 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) 0.00305 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATF5 NM_001193646.1 -?/. - c.-21230G>A r.(?) p.(=)
IL4I1 NM_001258017.1 -?/. - c.-227-3969C>T r.(=) p.(=)
NUP62 NM_153719.3 -?/. - c.1518C>T r.(?) p.(Cys506=)


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