Variant #0001040610 (NC_000015.9:g.78909414C>T, NM_000743.4:c.329G>A (CHRNA3))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.78909414C>T
DNA change (hg38) -
Published as CHRNA3(NM_000743.5):c.329G>A (p.(Arg110His))
ISCN -
DB-ID CHRNA3_000021
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) 0.00024 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNA3 NM_000743.4 ?/. - c.329G>A r.(?) p.(Arg110His)
CHRNA5 NM_000745.3 ?/. - c.*23819C>T r.(=) p.(=)


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