Variant #0000268579 (NC_000003.11:g.33155590_33155591dup, NM_006371.4:c.21_22dup (CRTAP))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33155590_33155591dup
DNA change (hg38) g.33114098_33114099dup
Published as CRTAP(NM_006371.5):c.21_22dupGG (p.A8Gfs*6)
ISCN -
DB-ID CRTAP_000011 See all 3 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRTAP NM_006371.4 +/. 1 c.21_22dup r.(?) p.(Ala8GlyfsTer6)


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