Variant #0000303019 (NC_000001.10:g.78407868G>C, NM_144573.3:c.1634G>C (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.78407868G>C
DNA change (hg38) g.77942183G>C
Published as NEXN(NM_144573.3):c.1634G>C (p.R545T)
ISCN -
DB-ID NEXN_000047
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
FUBP1 NM_003902.3 -?/. - c.*6583C>G r.(=) p.(=)
NEXN NM_144573.3 -?/. - c.1634G>C r.(?) p.(Arg545Thr)


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