Variant #0000866276 (NC_000019.9:g.5705841C>T, NM_004793.3:c.1309G>A (LONP1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.5705841C>T
DNA change (hg38) -
Published as LONP1(NM_001276479.1):c.1117G>A (p.(Val373Ile)), LONP1(NM_004793.3):c.1309G>A (p.V437I)
ISCN -
DB-ID LONP1_000023 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) 0.00307 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 2022-05-09 16:01:56 +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     
LONP1 NM_004793.3 -?/. - c.1309G>A r.(?) p.(Val437Ile)


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