Variant #0000333467 (NC_000023.10:g.24382417_24382428dup, NM_001136234.1:c.1540_1551dup (SUPT20HL1))

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.24382417_24382428dup
DNA change (hg38) g.24364300_24364311dup
Published as SUPT20HL1(NM_001136234.1):c.1496_1497insTGCTGCTGCTGC (p.(Ala502_Ala505dup)), SUPT20HL1(NM_001136234.2):c.1618_1629dupGCTGCTGCTGCT (p.A540_A543dup)
ISCN -
DB-ID SUPT20HL1_000009 See all 2 reported entries
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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUPT20HL1 NM_001136234.1 ?/. - c.1540_1551dup r.(?) p.(Ala514_Ala517dup)


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