Variant #0000890203 (NC_000011.9:g.819486T>C, NM_173584.3:c.-8604T>C (EFCAB4A))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.819486T>C
DNA change (hg38) -
Published as PNPLA2(NM_020376.4):c.-145-88T>C
ISCN -
DB-ID EFCAB4A_000018
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPLP2 NM_001004.3 -/. - c.*6650T>C r.(=) p.(=)
PNPLA2 NM_020376.3 -/. - c.-145-88T>C r.(=) p.(=)
EFCAB4A NM_173584.3 -/. - c.-8604T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.