Variant #0000542896 (NC_000011.9:g.125769318C>T, NC_000011.9(NM_031307.3):c.-46-3093G>A (PUS3))

Chromosome 11
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.125769318C>T
DNA change (hg38) g.125899423C>T
Published as HYLS1(NM_001134793.1):c.55C>T (p.R19*), HYLS1(NM_001134793.2):c.55C>T (p.(Arg19Ter))
ISCN -
DB-ID HYLS1_000005 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) 9.0E-5 View details
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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HYLS1 NM_001134793.1 ?/. - c.55C>T r.(?) p.(Arg19Ter)
DDX25 NM_013264.4 ?/. - c.-5095C>T r.(?) p.(=)
PUS3 NM_031307.3 ?/. - c.-46-3093G>A r.(=) p.(=)
HYLS1 NM_145014.2 ?/. - c.55C>T r.(?) p.(Arg19Ter)


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