Variant #0000951118 (NC_000018.9:g.2929103G>A, NM_014646.2:c.1510C>T (LPIN2))

Chromosome 18
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.2929103G>A
DNA change (hg38) -
Published as LPIN2(NM_001375808.2):c.1510C>T (p.(Leu504Phe)), LPIN2(NM_014646.2):c.1510C>T (p.L504F)
ISCN -
DB-ID LPIN2_000015 See all 5 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) 0.00262 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LPIN2 NM_014646.2 ?/. - c.1510C>T r.(?) p.(Leu504Phe)


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