Variant #0001050886 (NC_000002.11:g.175622321C>T, NM_001039523.2:c.392G>A (CHRNA1))

Chromosome 2
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.175622321C>T
DNA change (hg38) -
Published as CHRNA1(NM_000079.4):c.317G>A (p.(Trp106Ter)), CHRNA1(NM_001039523.2):c.392G>A (p.W131*), CHRNA1(NM_001039523.3):c.392G>A (p.W131*)
ISCN -
DB-ID CHRNA1_000052 See all 4 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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNA1 NM_000079.3 +?/. - c.317G>A r.(?) p.(Trp106Ter)
CHRNA1 NM_001039523.2 +?/. - c.392G>A r.(?) p.(Trp131Ter)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.