Variant #0000853165 (NC_000011.9:g.71806516C>T, NC_000011.9(NM_001145309.3):c.34+374C>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.71806516C>T
DNA change (hg38) -
Published as LRTOMT(NM_145309.5):c.529C>T (p.R177C)
ISCN -
DB-ID LAMTOR1_000014
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) 0.00026 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTOMT NM_001145309.3 ?/. - c.34+374C>T r.(=) p.(=)
NUMA1 NM_006185.2 ?/. - c.-15115G>A r.(?) p.(=)
ANAPC15 NM_014042.2 ?/. - c.*14411G>A r.(=) p.(=)
LAMTOR1 NM_017907.2 ?/. - c.*2352G>A r.(=) p.(=)


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