Variant #0000979922 (NC_000011.9:g.822397C>T, NM_173584.3:c.-5693C>T (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.822397C>T
DNA change (hg38) -
Published as PNPLA2(NM_020376.4):c.487C>T (p.(Arg163Cys))
ISCN -
DB-ID EFCAB4A_000023
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) 0.00012 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 2024-04-19 20:27:30 +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.*9561C>T r.(=) p.(=)
PNPLA2 NM_020376.3 ?/. - c.487C>T r.(?) p.(Arg163Cys)
EFCAB4A NM_173584.3 ?/. - c.-5693C>T r.(?) p.(=)


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