Variant #0000391982 (NC_000019.9:g.45208859G>C, NC_000019.9(NM_001039213.2):c.662-1G>C (CEACAM16))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45208859G>C
DNA change (hg38) g.44705589G>C
Published as -
ISCN -
DB-ID CEACAM16_000014 See all 2 reported entries
Variant remarks in vitro splicing minigene assay expressed in COS7 and HEK293 cells
Reference PubMed: Booth 2018, Journal: Booth 2018
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-07-23 13:43:11 +02:00 (CEST)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEACAM16 NM_001039213.2 +/. 4i c.662-1G>C r.[662_764del,622_940del] p.[Phe221Cysfs*16,Phe221_Ala313delinsSer]


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