Variant #0000929977 (NC_000011.9:g.71711615_71711617del, NM_001145309.3:c.-80859_-80857del (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.71711615_71711617del
DNA change (hg38) -
Published as IL18BP(NM_005699.3):c.235+12_235+14delAGT
ISCN -
DB-ID IL18BP_000007
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) 0.00171 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +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.-80859_-80857del r.(?) p.(=)
NUMA1 NM_006185.2 -?/. - c.*2956_*2958del r.(=) p.(=)
RNF121 NM_018320.4 -?/. - c.*4254_*4256del r.(=) p.(=)
IL18BP NM_173042.2 -?/. - c.235+12_235+14del r.(=) p.(=)


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