Variant #0000679328 (NC_000011.9:g.71715138C>T, NM_001145309.3:c.-77336C>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.71715138C>T
DNA change (hg38) -
Published as NUMA1(NM_001286561.1):c.6089G>A (p.R2030Q)
ISCN -
DB-ID IL18BP_000001
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) 0.00029 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.-77336C>T r.(?) p.(=)
NUMA1 NM_006185.2 ?/. - c.6131G>A r.(?) p.(Arg2044Gln)
IL18BP NM_173042.2 ?/. - c.*2231C>T r.(=) p.(=)


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