Variant #0000983608 (NC_000019.9:g.50412216_50412217insGTGGTG, NM_001193646.1:c.-20561_-20560insGTGGTG (ATF5))

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.50412216_50412217insGTGGTG
DNA change (hg38) -
Published as NUP62(NM_016553.5):c.850_851insCCACCA (p.(Ser283_Ser284insThrThr))
ISCN -
DB-ID ATF5_000021
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.-20561_-20560insGTGGTG r.(?) p.(=)
IL4I1 NM_001258017.1 ?/. - c.-227-4637_-227-4636insCCACCA r.(=) p.(=)
NUP62 NM_153719.3 ?/. - c.850_851insCCACCA r.(?) p.(Ser283_Ser284insThrThr)


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