Variant #0000970006 (NC_000019.9:g.5692207C>A, NM_004793.3:c.2716G>T (LONP1))

Chromosome 19
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.5692207C>A
DNA change (hg38) -
Published as LONP1(NM_004793.4):c.2716G>T (p.G906W)
ISCN -
DB-ID C19orf70_000012
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +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.2716G>T r.(?) p.(Gly906Trp)
RPL36 NM_015414.3 ?/. - c.*575C>A r.(=) p.(=)
HSD11B1L NM_198706.2 ?/. - c.*4251C>A r.(=) p.(=)
C19orf70 NM_205767.1 ?/. - c.-11710G>T r.(?) p.(=)


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