Variant #0000914374 (NC_000015.9:g.78893787G>A, NM_000743.4:c.1197C>T (CHRNA3))

Chromosome 15
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.78893787G>A
DNA change (hg38) -
Published as CHRNA3(NM_000743.5):c.1197C>T (p.D399=)
ISCN -
DB-ID CHRNA3_000013
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) 0.00364 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.1197C>T r.(?) p.(Asp399=)
CHRNA5 NM_000745.3 -/. - c.*8192G>A r.(=) p.(=)


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