Variant #0000718000 (NC_000002.11:g.175622321C>T, NM_001039523.2:c.392G>A (CHRNA1))

Chromosome 2
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.175622321C>T
DNA change (hg38) -
Published as 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 3 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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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)


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