Variant #0000291228 (NC_000011.9:g.71817250G>A, NM_001145309.3:c.352G>A (LRTOMT))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71817250G>A
DNA change (hg38) g.72106204G>A
Published as LRTOMT(NM_001145309.3):c.352G>A (p.V118I)
ISCN -
DB-ID LAMTOR1_000003
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) 0.00108 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 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     
LRTOMT NM_001145309.3 -/. - c.352G>A r.(?) p.(Val118Ile)
NUMA1 NM_006185.2 -/. - c.-25849C>T r.(?) p.(=)
ANAPC15 NM_014042.2 -/. - c.*3677C>T r.(=) p.(=)
LAMTOR1 NM_017907.2 -/. - c.-2980C>T r.(?) p.(=)


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