Variant #0000343762 (NC_000017.10:g.4802163dup, NM_000080.3:c.1353dup (CHRNE))

Chromosome 17
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.4802163dup
DNA change (hg38) g.4898868dup
Published as CHRNE(NM_000080.3):c.1353dupG (p.(Asn452fs))
ISCN -
DB-ID CHRNE_000154
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNE NM_000080.3 +/. - c.1353dup r.(?) p.(Asn452GlufsTer4)
C17orf107 NM_001145536.1 +/. - c.-895dup r.(?) p.(=)
MINK1 NM_015716.4 +/. - c.*1581dup r.(?) p.(=)


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