Variant #0000326078 (NC_000019.9:g.5691536C>T, NM_004793.3:c.*507G>A (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.5691536C>T
DNA change (hg38) g.5691525C>T
Published as RPL36(NM_015414.3):c.229-7C>T (p.(=))
ISCN -
DB-ID RPL36_000001
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) 0.00172 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LONP1 NM_004793.3 ?/. - c.*507G>A r.(=) p.(=)
RPL36 NM_015414.3 ?/. - c.229-7C>T r.(=) p.(=)
HSD11B1L NM_198706.2 ?/. - c.*3580C>T r.(=) p.(=)
C19orf70 NM_205767.1 ?/. - c.-11039G>A r.(?) p.(=)


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