Variant #0000297196 (NC_000011.9:g.824789T>C, NM_173584.3:c.-3301T>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.824789T>C
DNA change (hg38) g.824789T>C
Published as PNPLA2(NM_020376.4):c.1442T>C (p.L481P)
ISCN -
DB-ID PNPLA2_000007 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) 0.67167 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
RPLP2 NM_001004.3 -/. - c.*11953T>C r.(=) p.(=)
PNPLA2 NM_020376.3 -/. - c.1442T>C r.(?) p.(Leu481Pro)
EFCAB4A NM_173584.3 -/. - c.-3301T>C r.(?) p.(=)


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