Variant #0000890165 (NC_000011.9:g.71712936A>G, NM_001145309.3:c.-79538A>G (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.71712936A>G
DNA change (hg38) -
Published as IL18BP(NM_173044.2):c.486A>G (p.Q162=)
ISCN -
DB-ID IL18BP_000005
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 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 2022-11-01 13:01:21 +01:00 (CET)
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.-79538A>G r.(?) p.(=)
NUMA1 NM_006185.2 -?/. - c.*1637T>C r.(=) p.(=)
RNF121 NM_018320.4 -?/. - c.*5575A>G r.(=) p.(=)
IL18BP NM_173042.2 -?/. - c.*29A>G r.(=) p.(=)


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