Variant #0000966568 (NC_000011.9:g.71816060T>A, NC_000011.9(NM_001145309.3):c.83+2T>A (LRTOMT))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.71816060T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID LAMTOR1_000016
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
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.83+2T>A r.spl? p.?
NUMA1 NM_006185.2 +?/. - c.-24659A>T r.(?) p.(=)
ANAPC15 NM_014042.2 +?/. - c.*4867A>T r.(=) p.(=)
LAMTOR1 NM_017907.2 +?/. - c.-1790A>T r.(?) p.(=)


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