Variant #0000691182 (NC_000011.9:g.71711435G>A, NM_001145309.3:c.-81039G>A (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.71711435G>A
DNA change (hg38) -
Published as IL18BP(NM_005699.3):c.67G>A (p.V23I)
ISCN -
DB-ID IL18BP_000003
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) 0.00034 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 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.-81039G>A r.(?) p.(=)
NUMA1 NM_006185.2 -?/. - c.*3138C>T r.(=) p.(=)
RNF121 NM_018320.4 -?/. - c.*4074G>A r.(=) p.(=)
IL18BP NM_173042.2 -?/. - c.67G>A r.(?) p.(Val23Ile)


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