Variant #0000617898 (NC_000019.9:g.5696093A>C, NM_004793.3:c.1985T>G (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.5696093A>C
DNA change (hg38) g.5696082A>C
Published as LONP1(NM_004793.3):c.1985T>G (p.V662G), LONP1(NM_004793.4):c.1985T>G (p.(Val662Gly))
ISCN -
DB-ID RPL36_000008 See all 2 reported entries
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) 0.00052 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LONP1 NM_004793.3 ?/. - c.1985T>G r.(?) p.(Val662Gly)
RPL36 NM_015414.3 ?/. - c.*4461A>C r.(=) p.(=)


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