Variant #0001039636 (NC_000013.10:g.31035527_31035532del, NM_005800.4:c.-156735_-156730del (USPL1))

Chromosome 13
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.31035527_31035532del
DNA change (hg38) -
Published as HMGB1(NM_002128.7):c.621_626del (p.(Asp207_Glu208del))
ISCN -
DB-ID HMGB1_000007
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 2025-05-05 21:14:00 +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     
HMGB1 NM_002128.4 ?/. - c.621_626del r.(?) p.(Asp207_Glu208del)
USPL1 NM_005800.4 ?/. - c.-156735_-156730del r.(?) p.(=)


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