Variant #0000892420 (NC_000015.9:g.90209124T>C, NM_002666.4:c.1259A>G (PLIN1))

Chromosome 15
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.90209124T>C
DNA change (hg38) -
Published as PLIN1(NM_001145311.1):c.1259A>G (p.(Asp420Gly)), PLIN1(NM_002666.5):c.1259A>G (p.D420G)
ISCN -
DB-ID PLIN1_000064 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLIN1 NM_002666.4 ?/. - c.1259A>G r.(?) p.(Asp420Gly)


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