Variant #0000335261 (NC_000023.10:g.114541256_114541276dup, NM_016383.3:c.829_849dup (LUZP4))

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.114541256_114541276dup
DNA change (hg38) g.115306691_115306711dup
Published as LUZP4(NM_016383.3):c.824_825insCACTCAGAGAGATCTCGTGGC (p.(Val275_Thr276insThrGlnArgAspLeuValAla))
ISCN -
DB-ID LUZP4_000014
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     
LUZP4 NM_016383.3 ?/. - c.829_849dup r.(?) p.(Gln277_Thr283dup)


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