Variant #0000804004 (NC_000009.11:g.139569202T>A, NM_006412.3:c.646A>T (AGPAT2))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.139569202T>A
DNA change (hg38) -
Published as AGPAT2(NM_006412.3):c.646A>T (p.K216*), AGPAT2(NM_006412.4):c.646A>T (p.K216*)
ISCN -
DB-ID AGPAT2_000014 See all 3 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) 0.00038 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGPAT2 NM_006412.3 +/. - c.646A>T r.(?) p.(Lys216Ter)
EGFL7 NM_016215.4 +/. - c.*2464T>A r.(=) p.(=)


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