Variant #0000622718 (NC_000011.9:g.71817089T>G, NM_001145309.3:c.191T>G (LRTOMT))

Chromosome 11
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.71817089T>G
DNA change (hg38) g.72106043T>G
Published as LRTOMT(NM_001145309.4):c.191T>G (p.V64G)
ISCN -
DB-ID LAMTOR1_000009 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) 5.0E-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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTOMT NM_001145309.3 ?/. - c.191T>G r.(?) p.(Val64Gly)
NUMA1 NM_006185.2 ?/. - c.-25688A>C r.(?) p.(=)
ANAPC15 NM_014042.2 ?/. - c.*3838A>C r.(=) p.(=)
LAMTOR1 NM_017907.2 ?/. - c.-2819A>C r.(?) p.(=)


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