Variant #0000951363 (NC_000019.9:g.5687813G>A, NM_004793.3:c.*4230C>T (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.5687813G>A
DNA change (hg38) -
Published as HSD11B1L(NM_001267868.1):c.859G>A (p.(Val287Met))
ISCN -
DB-ID C19orf70_000010
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) 0.00023 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 2023-11-27 17:35:39 +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.*4230C>T r.(=) p.(=)
RPL36 NM_015414.3 -?/. - c.-2706G>A r.(?) p.(=)
HSD11B1L NM_198706.2 -?/. - c.718G>A r.(?) p.(Val240Met)
C19orf70 NM_205767.1 -?/. - c.-7316C>T r.(?) p.(=)


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