Variant #0000619429 (NC_000023.10:g.24329896_24329907dup, NM_001136233.1:c.1537_1548dup (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.24329896_24329907dup
DNA change (hg38) g.24311779_24311790dup
Published as SUPT20HL2(NM_001136233.1):c.1548_1549insGCTGCTCCTGCT (p.(Ala513_Ala516dup))
ISCN -
DB-ID SUPT20HL2_000037
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 2020-03-23 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.1537_1548dup r.(?) p.(Ala513_Ala516dup)


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