Variant #0001026695 (NC_000016.9:g.31195253T>A, NM_004960.3:c.265T>A (FUS))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31195253T>A
DNA change (hg38) -
Published as FUS(NM_004960.3):c.265T>A (p.S89T), FUS(NM_004960.4):c.265T>A (p.S89T)
ISCN -
DB-ID FUS_000207 See all 2 reported entries
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUS NM_004960.3 ?/. - c.265T>A r.(?) p.(Ser89Thr)


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