Variant #0000094338 (NC_000023.10:g.68049516_68049525delinsTTGGGCGCCC, NM_004429.4:c.-104_-95delinsTTGGGCGCCC (EFNB1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.68049516_68049525delinsTTGGGCGCCC
DNA change (hg38) g.68829673_68829682delinsTTGGGCGCCC
Published as c.[-104A>T;-95T>C]
ISCN -
DB-ID EFNB1_000046
Variant remarks luciferase assay shows raised protein translation (1.6)
Reference PubMed: Twigg 2013, Journal: Twigg 2013
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-04-08 19:03:59 +02:00 (CEST)
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     
EFNB1 NM_004429.4 -?/. 1 c.-104_-95delinsTTGGGCGCCC r.-104_-95delinsuugggcgccc p.(=)


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