Variant #0000333496 (NC_000023.10:g.24382401_24382402insATT, NM_001136234.1:c.1524_1525insATT (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.24382401_24382402insATT
DNA change (hg38) g.24364284_24364285insATT
Published as SUPT20HL1(NM_001136234.1):c.1523_1524insTAT (p.(Ala508_Ala509insIle))
ISCN -
DB-ID SUPT20HL1_000030
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     
SUPT20HL1 NM_001136234.1 ?/. - c.1524_1525insATT r.(?) p.(Ala508_Ala509insIle)


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