Variant #0000979434 (NC_000011.9:g.125770159_125770161del, NC_000011.9(NM_031307.3):c.-47+2907_-47+2909del (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.125770159_125770161del
DNA change (hg38) -
Published as HYLS1(NM_001134793.2):c.896_898del (p.(Ser299del))
ISCN -
DB-ID HYLS1_000019
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 2024-04-19 20:27:30 +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.896_898del r.(?) p.(Ser299*)
DDX25 NM_013264.4 ?/. - c.-4254_-4252del r.(?) p.(=)
PUS3 NM_031307.3 ?/. - c.-47+2907_-47+2909del r.(=) p.(=)
HYLS1 NM_145014.2 ?/. - c.896_898del r.(?) p.(Ser299*)


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