Variant #0000619428 (NC_000023.10:g.24329890_24329891insCAGC, NM_001136233.1:c.1542_1543insGCTG (SUPT20HL2))

Chromosome X
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.24329890_24329891insCAGC
DNA change (hg38) g.24311773_24311774insCAGC
Published as SUPT20HL2(NM_001136233.1):c.1542_1543insGCTG (p.(Pro515AlafsTer30))
ISCN -
DB-ID SUPT20HL2_000036
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-17 21:20:16 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUPT20HL2 NM_001136233.1 -?/. - c.1542_1543insGCTG r.(?) p.(Pro515AlafsTer30)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.