Variant #0000728789 (NC_000023.10:g.24383328_24383336dup, NM_001136234.1:c.2451_2459dup (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.24383328_24383336dup
DNA change (hg38) -
Published as SUPT20HL1(NM_001136234.2):c.2529_2537dupGCCGCAGCA (p.Q843_Q845dup)
ISCN -
DB-ID SUPT20HL1_000066
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUPT20HL1 NM_001136234.1 ?/. - c.2451_2459dup r.(?) p.(Gln817_Gln819dup)


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