Variant #0001056441 (NC_000019.9:g.5692223G>C, NC_000019.9(NM_004793.3):c.2704-4C>G (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.5692223G>C
DNA change (hg38) -
Published as LONP1(NM_004793.4):c.2704-4C>G
ISCN -
DB-ID chr19_008559
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 2025-11-01 13:22:20 +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.2704-4C>G r.spl? p.?
RPL36 NM_015414.3 -?/. - c.*591G>C r.(=) p.(=)
HSD11B1L NM_198706.2 -?/. - c.*4267G>C r.(=) p.(=)
C19orf70 NM_205767.1 -?/. - c.-11726C>G r.(?) p.(=)


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