Variant #0000563055 (NC_000017.10:g.7359942G>T, NM_000747.2:c.1406G>T (CHRNB1))

Chromosome 17
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.7359942G>T
DNA change (hg38) g.7456623G>T
Published as CHRNB1(NM_000747.3):c.1406G>T (p.(Arg469Leu))
ISCN -
DB-ID CHRNB1_000027
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) 9.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNB1 NM_000747.2 ?/. - c.1406G>T r.(?) p.(Arg469Leu)
SLC35G6 NM_001102614.1 ?/. - c.-24894G>T r.(?) p.(=)
ZBTB4 NM_020899.3 ?/. - c.*5317C>A r.(=) p.(=)


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