Variant #0000340168 (NC_000017.10:g.4802329G>A, NM_000080.3:c.1293C>T (CHRNE))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4802329G>A
DNA change (hg38) g.4899034G>A
Published as -
ISCN -
DB-ID CHRNE_000157
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) 0.14649 View details
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 13:42:29 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNE NM_000080.3 -/. - c.1293C>T r.(?) p.(Ala431=)
C17orf107 NM_001145536.1 -/. - c.-729G>A r.(?) p.(=)
MINK1 NM_015716.4 -/. - c.*1747G>A r.(=) p.(=)


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