Variant #0000852798 (NC_000011.9:g.125769536G>T, NC_000011.9(NM_031307.3):c.-46-3311C>A (PUS3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.125769536G>T
DNA change (hg38) -
Published as HYLS1(NM_145014.2):c.273G>T (p.K91N)
ISCN -
DB-ID HYLS1_000012
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) 0.00211 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 2022-05-09 15:40:45 +02:00 (CEST)
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.273G>T r.(?) p.(Lys91Asn)
DDX25 NM_013264.4 -/. - c.-4877G>T r.(?) p.(=)
PUS3 NM_031307.3 -/. - c.-46-3311C>A r.(=) p.(=)
HYLS1 NM_145014.2 -/. - c.273G>T r.(?) p.(Lys91Asn)


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