Variant #0000563054 (NC_000017.10:g.7359154T>C, NM_000747.2:c.1259T>C (CHRNB1))

Chromosome 17
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.7359154T>C
DNA change (hg38) g.7455835T>C
Published as CHRNB1(NM_000747.3):c.1259T>C (p.(Ile420Thr))
ISCN -
DB-ID CHRNB1_000014 See all 4 reported entries
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) 0.00283 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 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNB1 NM_000747.2 -?/. - c.1259T>C r.(?) p.(Ile420Thr)
SLC35G6 NM_001102614.1 -?/. - c.-25682T>C r.(?) p.(=)
ZBTB4 NM_020899.3 -?/. - c.*6105A>G r.(=) p.(=)


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