Variant #0000736813 (NC_000017.10:g.7352014C>T)

Individual ID 00335954
Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS (!)
DNA change (genomic) (Relative to hg19 / GRCh37) g.7352014C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CHRNB1_000004 See all 4 reported entries
Variant remarks ACMG: PM2_Sup, PM3, PP3: class 3; / NM_000747.3:c.727C>T chr17:7352014 p.(Arg243Cys)
Reference PMID: 29395675; PMID: 17686188
ClinVar ID ClinVar-000448999
dbSNP ID -
Origin Germline
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2021-03-10 14:49:45 +01:00 (CET)
Date last edited 2021-03-17 14:59:14 +01:00 (CET)
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000337184 DNA SEQ-NG-I - - CHRNB1 2 Andreas Laner


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.