Variant #0000949609 (NC_000011.9:g.125769294del, NC_000011.9(NM_031307.3):c.-46-3069del (PUS3))

Chromosome 11
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.125769294del
DNA change (hg38) -
Published as HYLS1(NM_145014.2):c.31delT (p.W11Gfs*46)
ISCN -
DB-ID HYLS1_000015
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) 1.0E-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 2023-11-27 17:35:39 +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     
HYLS1 NM_001134793.1 +/. - c.31del r.(?) p.(Trp11Glyfs*46)
DDX25 NM_013264.4 +/. - c.-5119del r.(?) p.(=)
PUS3 NM_031307.3 +/. - c.-46-3069del r.(=) p.(=)
HYLS1 NM_145014.2 +/. - c.31del r.(?) p.(Trp11Glyfs*46)


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