Variant #0000616796 (NC_000017.10:g.7217654_7217656del, NM_032442.2:c.*1788_*1790del (NEURL4))

Chromosome 17
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.7217654_7217656del
DNA change (hg38) g.7314335_7314337del
Published as -
ISCN -
DB-ID EIF5A_000002
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF5A NM_001143760.1 ?/. - c.*2525_*2527del r.(=) p.(=)
GPS2 NM_004489.4 ?/. - c.273_275del r.(?) p.(Lys92del)
NEURL4 NM_032442.2 ?/. - c.*1788_*1790del r.(=) p.(=)


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