Variant #0000848861 (NC_000001.10:g.78408163_78408168del, NM_144573.3:c.1677_1682del (NEXN))

Chromosome 1
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.78408163_78408168del
DNA change (hg38) -
Published as NEXN(NM_144573.3):c.1677_1682delGGAGGA (p.E561_E562del), NEXN(NM_144573.4):c.1677_1682delGGAGGA (p.E561_E562del)
ISCN -
DB-ID NEXN_000050 See all 3 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.*6291_*6296del r.(=) p.(=)
NEXN NM_144573.3 -?/. - c.1677_1682del r.(?) p.(Glu561_Glu562del)


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