Variant #0000804979 (NC_000011.9:g.125761395dup, NM_031307.3:c.*2301dup (PUS3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.125761395dup
DNA change (hg38) -
Published as HYLS1(NM_145014.2):c.-81+28dupA
ISCN -
DB-ID HYLS1_000011
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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.-26+28dup r.(=) p.(=)
PUS3 NM_031307.3 -?/. - c.*2301dup r.(?) p.(=)
HYLS1 NM_145014.2 -?/. - c.-81+28dup r.(=) p.(=)


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