Variant #0000335872 (NC_000023.10:g.150156375_150156380del, NM_005342.2:c.591_596del (HMGB3))

Chromosome X
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.150156375_150156380del
DNA change (hg38) g.150987902_150987907del
Published as HMGB3(NM_005342.2):c.574_579del (p.(Glu194_Glu195del))
ISCN -
DB-ID HMGB3_000008
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMGB3 NM_005342.2 ?/. - c.591_596del r.(?) p.(Glu197_Glu198del)


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