Variant #0000170190 (NC_000001.10:g.26140389C>T, NM_020451.2:c.1405C>T (SEPN1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.26140389C>T
DNA change (hg38) g.25813898C>T
Published as -
ISCN -
DB-ID SEPN1_000026 See all 11 reported entries
Variant remarks cloned in pUGA2SECIS; Sec in vitro insertion efficiency unaffected
Reference PubMed: Maiti 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-02-21 17:28:23 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEPN1 NM_020451.2 ?/. 11 c.1405C>T r.(?) p.(Arg469Trp)


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