Variant #0000605975 (NC_000001.10:g.78408435_78408437del, NM_144573.3:c.1949_1951del (NEXN))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78408435_78408437del
DNA change (hg38) g.77942750_77942752del
Published as NEXN(NM_144573.4):c.1949_1951delGAG (p.G650del)
ISCN -
DB-ID FUBP1_000012 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 14:54:23 +01:00 (CET)
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.*6018_*6020del r.(=) p.(=)
NEXN NM_144573.3 +?/. - c.1949_1951del r.(?) p.(Gly650del)


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