Variant #0000260668 (NC_000009.11:g.139571989G>A, NM_006412.3:c.202C>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.139571989G>A
DNA change (hg38) g.136677537G>A
Published as AGPAT2(NM_006412.3):c.202C>T (p.R68*), AGPAT2(NM_006412.4):c.202C>T (p.R68*)
ISCN -
DB-ID AGPAT2_000003 See all 5 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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGPAT2 NM_006412.3 +/. - c.202C>T r.(?) p.(Arg68Ter)
EGFL7 NM_016215.4 +/. - c.*5251G>A r.(=) p.(=)


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