Variant #0000323982 (NC_000015.9:g.40328616_40328624del, NM_001013703.2:c.*1331_*1339del (EIF2AK4))

Chromosome 15
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.40328616_40328624del
DNA change (hg38) g.40036415_40036423del
Published as SRP14(NM_003134.4):c.340_348del (p.(Ala114_Ala116del))
ISCN -
DB-ID SRP14_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF2AK4 NM_001013703.2 ?/. - c.*1331_*1339del r.(=) p.(=)
SRP14 NM_003134.4 ?/. - c.340_348del r.(?) p.(Ala114_Ala116del)


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