Variant #0000870336 (NC_000002.11:g.29296762A>G, NM_001029883.2:c.366T>C (C2orf71))

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.29296762A>G
DNA change (hg38) -
Published as c.366C>T
ISCN -
DB-ID C2orf71_000213
Variant remarks -
Reference PubMed: Audo 2011
ClinVar ID -
dbSNP ID rs17007546
Origin Unknown
Segregation -
Frequency 1/418 patient chromosomes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00242 View details
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2022-06-18 03:05:08 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2orf71 NM_001029883.2 -/. 1 c.366T>C r.(=) p.(=)


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