Variant #0000854979 (NC_000017.10:g.4804366G>A, NM_000080.3:c.721C>T (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.4804366G>A
DNA change (hg38) -
Published as CHRNE(NM_000080.3):c.721C>T (p.(Leu241Phe))
ISCN -
DB-ID CHRNE_000002 See all 5 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNE NM_000080.3 +/. - c.721C>T r.(?) p.(Leu241Phe)
C17orf107 NM_001145536.1 +/. - c.*538G>A r.(=) p.(=)
MINK1 NM_015716.4 +/. - c.*3784G>A r.(=) p.(=)


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