Variant #0000302862 (NC_000017.10:g.40688571_40688573delinsCCC, NM_000263.3:c.281_283delinsCCC (NAGLU))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40688571_40688573delinsCCC
DNA change (hg38) g.42536553_42536555delinsCCC
Published as NAGLU(NM_000263.3):c.281_283delGCGinsCCC (p.R94_D95delinsPH)
ISCN -
DB-ID NAGLU_000011
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 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     
NAGLU NM_000263.3 +?/. - c.281_283delinsCCC r.(?) p.(Arg94_Asp95delinsProHis)


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