Variant #0000244080 (NC_000016.9:g.31103210_31103221del, NC_000016.9(NM_004960.3):c.515_523+3del (FUS))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31103210_31103221del
DNA change (hg38) g.31091889_31091900del
Published as -
ISCN -
DB-ID FUS_000110 See all 2 reported entries
Variant remarks Observed in 1 patient, not in controls. However, other variation at this hexanucleotide repeat was observed in controls. /r/Dodecanucleotide deletion at intron 5 splice donor site predicting alternative splicing resulting in deletion of four amino acids
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Marc Cruts
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-05-01 13:44:57 +02:00 (CEST)
Date last edited 2019-07-16 18:35:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUS NM_004960.3 -/? 5_5i c.515_523+3del r.(?) p.?


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