Variant #0000809070 (NC_000019.9:g.5692093C>G, NM_004793.3:c.2830G>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.5692093C>G
DNA change (hg38) -
Published as LONP1(NM_001276479.1):c.2638G>C (p.(Asp880His))
ISCN -
DB-ID C19orf70_000009
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) 1.0E-5 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 2021-09-17 14:40:49 +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.2830G>C r.(?) p.(Asp944His)
RPL36 NM_015414.3 -?/. - c.*461C>G r.(=) p.(=)
HSD11B1L NM_198706.2 -?/. - c.*4137C>G r.(=) p.(=)
C19orf70 NM_205767.1 -?/. - c.-11596G>C r.(?) p.(=)


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