Variant #0000991193 (NC_000001.10:g.36026326_36026342dup, NM_014284.2:c.574_590dup (NCDN))

Chromosome 1
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.36026326_36026342dup
DNA change (hg38) -
Published as NCDN(NM_014284.2):c.574_590dupTTTGACCAGGCCCTGGC (p.(Leu199fs))
ISCN -
DB-ID KIAA0319L_000004
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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NCDN NM_014284.2 +?/. - c.574_590dup r.(?) p.(Leu199Thrfs*81)
KIAA0319L NM_024874.4 +?/. - c.-3559_-3543dup r.(?) p.(=)


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