Variant #0000925019 (NC_000009.11:g.139571472G>T, NM_006412.3:c.433C>A (AGPAT2))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.139571472G>T
DNA change (hg38) -
Published as AGPAT2(NM_001012727.1):c.433C>A (p.(Arg145Ser)), AGPAT2(NM_006412.3):c.433C>A (p.R145S)
ISCN -
DB-ID AGPAT2_000002 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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGPAT2 NM_006412.3 ?/. - c.433C>A r.(?) p.(Arg145Ser)
EGFL7 NM_016215.4 ?/. - c.*4734G>T r.(=) p.(=)


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