Variant #0000254864 (NC_000006.11:g.131997885A>G, NM_001145659.1:c.*31939T>C (CTAGE9))

Chromosome 6
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.131997885A>G
DNA change (hg38) g.131676745A>G
Published as ENPP3(NM_005021.4):c.882A>G (p.P294=)
ISCN -
DB-ID ENPP3_000003
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) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-22 10:22:13 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTAGE9 NM_001145659.1 -?/. - c.*31939T>C r.(=) p.(=)
ENPP3 NM_005021.3 -?/. - c.882A>G r.(?) p.(Pro294=)
OR2A4 NM_030908.1 -?/. - c.*23724T>C r.(=) p.(=)


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