Variant #0000244083 (NC_000016.9:g.31103919_31103924del, NM_004960.3:c.(681_686del) (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.31103919_31103924del
DNA change (hg38) g.31092598_31092603del
Published as -
ISCN -
DB-ID FUS_000114
Variant remarks Observed in 4 ALS patients, not in controls. Howerver, other variation at this trinucleotide repeat was observed in controls. /r/Hexanucleotide deletion in coding region predicting a deletion of two 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 2020-07-09 15:44:16 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUS NM_004960.3 -/? 6 c.(681_686del) r.(?) p.(Gly230_Gly231del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.