Variant #0001038754 (NC_000011.9:g.71717300C>T, NM_001145309.3:c.-75174C>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.71717300C>T
DNA change (hg38) -
Published as NUMA1(NM_006185.4):c.5473G>A (p.(Val1825Met))
ISCN -
DB-ID IL18BP_000009
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) 0.00576 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.-75174C>T r.(?) p.(=)
NUMA1 NM_006185.2 -?/. - c.5473G>A r.(?) p.(Val1825Met)
IL18BP NM_173042.2 -?/. - c.*4393C>T r.(=) p.(=)


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