Variant #0000895142 (NC_000019.9:g.5694903C>G, NM_004793.3:c.2023G>C (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.5694903C>G
DNA change (hg38) -
Published as LONP1(NM_001276479.1):c.1831G>C (p.(Val611Leu))
ISCN -
DB-ID RPL36_000014
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) 0.00731 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 2022-11-01 13:41:49 +01:00 (CET)
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.2023G>C r.(?) p.(Val675Leu)
RPL36 NM_015414.3 -?/. - c.*3271C>G r.(=) p.(=)


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