Variant #0000291229 (NC_000011.9:g.71800166G>A, NM_001145309.3:c.-367G>A (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.71800166G>A
DNA change (hg38) g.72089120G>A
Published as LRTOMT(NM_001271471.2):c.37G>A (p.E13K)
ISCN -
DB-ID LRTOMT_000001
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) 0.00466 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTOMT NM_001145309.3 ?/. - c.-367G>A r.(?) p.(=)
NUMA1 NM_006185.2 ?/. - c.-8765C>T r.(?) p.(=)
ANAPC15 NM_014042.2 ?/. - c.*20761C>T r.(=) p.(=)
LAMTOR1 NM_017907.2 ?/. - c.*8702C>T r.(=) p.(=)
LRTOMT NM_145309.3 ?/. - c.37G>A r.(?) p.(Glu13Lys)


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