Variant #0000722416 (NC_000009.11:g.139569261T>C, NC_000009.11(NM_006412.3):c.589-2A>G (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.139569261T>C
DNA change (hg38) -
Published as AGPAT2(NM_006412.4):c.589-2A>G
ISCN -
DB-ID EGFL7_000003 See all 2 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) 0.0001 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGPAT2 NM_006412.3 +/. - c.589-2A>G r.spl? p.?
EGFL7 NM_016215.4 +/. - c.*2523T>C r.(=) p.(=)


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