Variant #0000545649 (NC_000011.9:g.71817260A>C, NC_000011.9(NM_001145309.3):c.358+4A>C (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.71817260A>C
DNA change (hg38) g.72106214A>C
Published as -
ISCN -
DB-ID LAMTOR1_000004 See all 2 reported entries
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) 5.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 10:16:49 +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.358+4A>C r.spl? p.?
NUMA1 NM_006185.2 +?/. - c.-25859T>G r.(?) p.(=)
ANAPC15 NM_014042.2 +?/. - c.*3667T>G r.(=) p.(=)
LAMTOR1 NM_017907.2 +?/. - c.-2990T>G r.(?) p.(=)


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