Variant #0000164567 (NC_000007.13:g.144098161del, NM_001080413.3:c.822del (NOBOX))

Chromosome 7
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.144098161del
DNA change (hg38) g.144401068del
Published as -
ISCN -
DB-ID NOBOX_000001 See all 2 reported entries
Variant remarks cDNA expression cloning in 293FT cells showed normal protein expression (truncated), reduced (0.2) GDF9 promoter activation and reduced gene expression activation of CPSF4L, MYOT,
RFPL4A, UNC13C, GDF9, NLRP14 and RSPO2
Reference PubMed: Li 2017
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 2017-03-24 15:25:24 +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     
NOBOX NM_001080413.3 +/. 4 c.822del r.(?) p.Thr275Hisfs*13


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