Variant #0000508467 (NC_000001.10:g.78408364_78408366del, NM_144573.3:c.1878_1880del (NEXN))

Chromosome 1
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.78408364_78408366del
DNA change (hg38) g.77942679_77942681del
Published as NEXN(NM_144573.3):c.1878_1880delAGA (p.E626del)
ISCN -
DB-ID NEXN_000052 See all 2 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUBP1 NM_003902.3 ?/. - c.*6088_*6090del r.(=) p.(=)
NEXN NM_144573.3 ?/. - c.1878_1880del r.(?) p.(Glu626del)


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