Variant #0000853166 (NC_000011.9:g.71817015A>G, NM_001145309.3:c.117A>G (LRTOMT))

Chromosome 11
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.71817015A>G
DNA change (hg38) -
Published as LRTOMT(NM_001145309.3):c.117A>G (p.A39=)
ISCN -
DB-ID LAMTOR1_000015
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTOMT NM_001145309.3 -?/. - c.117A>G r.(?) p.(Ala39=)
NUMA1 NM_006185.2 -?/. - c.-25614T>C r.(?) p.(=)
ANAPC15 NM_014042.2 -?/. - c.*3912T>C r.(=) p.(=)
LAMTOR1 NM_017907.2 -?/. - c.-2745T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.