Variant #0000691185 (NC_000011.9:g.71804714C>T, NM_001145309.3:c.-149C>T (LRTOMT))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71804714C>T
DNA change (hg38) -
Published as LRTOMT(NM_001271471.2):c.255C>T (p.D85=)
ISCN -
DB-ID LAMTOR1_000011
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) 0.00311 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 2020-09-15 15:50:26 +02:00 (CEST)
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.-149C>T r.(?) p.(=)
NUMA1 NM_006185.2 -?/. - c.-13313G>A r.(?) p.(=)
ANAPC15 NM_014042.2 -?/. - c.*16213G>A r.(=) p.(=)
LAMTOR1 NM_017907.2 -?/. - c.*4154G>A r.(=) p.(=)
LRTOMT NM_145309.3 -?/. - c.255C>T r.(?) p.(Asp85=)


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