Variant #0000328931 (NC_000022.10:g.24041029_24041041del, NC_000022.10(NR_024448.2):n.1162+1872_1162+1884del (GUSBP11))

Chromosome 22
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.24041029_24041041del
DNA change (hg38) g.23698842_23698854del
Published as RGL4(NM_153615.1):c.1383-2_1393del (p.?)
ISCN -
DB-ID GUSBP11_000003
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGL4 NM_153615.1 ?/. - c.1383-2_1393del r.spl? p.?
GUSBP11 NR_024448.2 ?/. - n.1162+1872_1162+1884del r.(?) -


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