Variant #0000222712 (NC_000006.11:g.(117996640_118029751dup), NM_138459.3:c.(-194_*1573dup) (NUS1))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(117996640_118029751dup)
DNA change (hg38) -
Published as g.95751061_95751062ins[95751062_95751078;G;NM_138459.2:c.-194_*1573;AAAAAAAAAAAAAAAAA]
ISCN -
DB-ID NUS1_000001
Variant remarks the additional copy of this sequence is inserted in SLC25A13 intron 16 on chromosome 7
Reference PubMed: Tabata 2008, Journal: Tabata 2008
ClinVar ID -
dbSNP ID -
Origin DUPLICATE record
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 2017-11-02 08:53:56 +01:00 (CET)
Date last edited 2017-11-02 08:54:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUS1 NM_138459.3 +/+ 1_5 c.(-194_*1573dup) - -


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