Variant #0000328929 (NC_000022.10:g.24035006_24035017dup, NC_000022.10(NR_024448.2):n.2561+1293_2561+1304dup (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.24035006_24035017dup
DNA change (hg38) g.23692819_23692830dup
Published as RGL4(NM_153615.1):c.519_520insCCAGCACCAGCA (p.(Gly173_Pro174insProAlaProAla))
ISCN -
DB-ID GUSBP11_000001
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.524_535dup r.(?) p.(Ala175_Pro178dup)
GUSBP11 NR_024448.2 ?/. - n.2561+1293_2561+1304dup r.(?) -


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