Variant #0000452740 (NC_000002.11:g.152573981A>G, NM_001271208.1:c.771T>C (NEB))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.152573981A>G
DNA change (hg38) g.151717467A>G
Published as -
ISCN -
DB-ID NEB_000102
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs4611637
Origin Germline
Segregation -
Frequency 0.27-0.88
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.75553 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-08-20 15:51:50 +02:00 (CEST)
Date last edited 2020-09-25 17:50:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
NEB NM_001271208.1 -/. 10 c.771T>C - r.(?) p.(?)


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