Variant #0000244081 (NC_000016.9:g.31103924_31103925insGGCGGC, NM_004960.3:c.(681_686dup) (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.31103924_31103925insGGCGGC
DNA change (hg38) g.31092603_31092604insGGCGGC
Published as -
ISCN -
DB-ID FUS_000120
Variant remarks Observed in 1 control, not in ALS patients. /r/Hexanucleotide insertion in coding region predicting an insertion 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 15:46:55 +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_686dup) r.(?) p.(Gly230_Gly231dup)


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