Variant #0000892295 (NC_000015.9:g.78913087_78913089dup, NM_000743.4:c.67_69dup (CHRNA3))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.78913087_78913089dup
DNA change (hg38) -
Published as CHRNA3(NM_000743.5):c.67_69dupCTG (p.L23dup)
ISCN -
DB-ID CHRNA3_000012
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +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.67_69dup r.(?) p.(Leu23dup)
CHRNA5 NM_000745.3 -?/. - c.*27492_*27494dup r.(=) p.(=)
CHRNB4 NM_000750.3 -?/. - c.*4405_*4407dup r.(=) p.(=)


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