Variant #0000333454 (NC_000023.10:g.24329920_24329925dup, NM_001136233.1:c.1531_1536dup (SUPT20HL2))

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.24329920_24329925dup
DNA change (hg38) g.24311803_24311808dup
Published as SUPT20HL2(NM_001136233.1):c.1536_1537insCCTGCT (p.(Pro511_Ala512dup))
ISCN -
DB-ID SUPT20HL2_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 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     
SUPT20HL2 NM_001136233.1 ?/. - c.1531_1536dup r.(?) p.(Pro511_Ala512dup)


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