Variant #0000613690 (NC_000011.9:g.71819657C>T, NM_001145309.3:c.562C>T (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.71819657C>T
DNA change (hg38) g.72108611C>T
Published as LRTOMT(NM_001145309.3):c.562C>T (p.L188F)
ISCN -
DB-ID LAMTOR1_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) Retrieve
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 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     
LRTOMT NM_001145309.3 ?/. - c.562C>T r.(?) p.(Leu188Phe)
NUMA1 NM_006185.2 ?/. - c.-28256G>A r.(?) p.(=)
ANAPC15 NM_014042.2 ?/. - c.*1270G>A r.(=) p.(=)
LAMTOR1 NM_017907.2 ?/. - c.-5387G>A r.(?) p.(=)


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