Variant #0000998069 (NC_000010.10:g.104263946_104263962del, NM_016169.3:c.37_53del (SUFU))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.104263946_104263962del
DNA change (hg38) -
Published as SUFU(NM_016169.3):c.37_53delACCGCGCCCCCGGCCCC (p.(Thr13fs))
ISCN -
DB-ID SUFU_000057 See all 3 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTR1A NM_005736.3 +/. - c.-1544_-1528del r.(?) p.(=)
SUFU NM_016169.3 +/. - c.37_53del r.(?) p.(Thr13Trpfs*29)


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