Variant #0000568091 (NC_000019.9:g.50435887_50435890del, NM_001193646.1:c.387_390del (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.50435887_50435890del
DNA change (hg38) g.49932630_49932633del
Published as ATF5(NM_001193646.1):c.387_390del (p.(Leu130HisfsTer93))
ISCN -
DB-ID ATF5_000013
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) 9.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 11:04:16 +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.387_390del r.(?) p.(Leu130HisfsTer93)
IL4I1 NM_001258017.1 ?/. - c.-3633_-3630del r.(?) p.(=)
NUP62 NM_153719.3 ?/. - c.-3540_-3537del r.(?) p.(=)


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