Variant #0000557958 (NC_000016.9:g.31195715_31195720dup, NC_000016.9(NM_004960.3):c.521_523+3dup (FUS))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31195715_31195720dup
DNA change (hg38) g.31184394_31184399dup
Published as FUS(NM_004960.3):c.520_525dupGGAGGT (p.G174_G175dup)
ISCN -
DB-ID FUS_000182
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-09 15:51:41 +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 -?/. - c.521_523+3dup r.spl? p.?


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