Variant #0000345396 (NC_000017.10:g.4802525_4802531dup, NM_000080.3:c.1181_1187dup (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.4802525_4802531dup
DNA change (hg38) g.4899230_4899236dup
Published as -
ISCN -
DB-ID CHRNE_000158
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 2020-07-11 13:42:54 +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.1181_1187dup r.(?) p.(Glu396AspfsTer3)
C17orf107 NM_001145536.1 +/. - c.-533_-527dup r.(?) p.(=)
MINK1 NM_015716.4 +/. - c.*1943_*1949dup r.(=) p.(=)


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