Variant #0000249423 (NC_000019.9:g.50413019A>C, NM_001193646.1:c.-19758A>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.50413019A>C
DNA change (hg38) g.49909762A>C
Published as NUP62(NM_016553.5):c.46T>G (p.F16V)
ISCN -
DB-ID IL4I1_000011
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_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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATF5 NM_001193646.1 -?/. - c.-19758A>C r.(?) p.(=)
IL4I1 NM_001258017.1 -?/. - c.-227-5441T>G r.(=) p.(=)
NUP62 NM_153719.3 -?/. - c.46T>G r.(?) p.(Phe16Val)


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