Variant #0000853205 (NC_000011.9:g.821676G>A, NM_173584.3:c.-6414G>A (EFCAB4A))

Chromosome 11
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.821676G>A
DNA change (hg38) -
Published as PNPLA2(NM_020376.3):c.236G>A (p.R79Q, p.(Arg79Gln)), PNPLA2(NM_020376.4):c.236G>A (p.R79Q)
ISCN -
DB-ID PNPLA2_000002 See all 4 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) 0.00067 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 2022-05-09 15:40:45 +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     
RPLP2 NM_001004.3 ?/. - c.*8840G>A r.(=) p.(=)
PNPLA2 NM_020376.3 ?/. - c.236G>A r.(?) p.(Arg79Gln)
EFCAB4A NM_173584.3 ?/. - c.-6414G>A r.(?) p.(=)


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