Variant #0000691183 (NC_000011.9:g.71712876C>A, NM_001145309.3:c.-79598C>A (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.71712876C>A
DNA change (hg38) -
Published as IL18BP(NM_173042.2):c.554C>A (p.S185Y)
ISCN -
DB-ID IL18BP_000004
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) 0.00023 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.-79598C>A r.(?) p.(=)
NUMA1 NM_006185.2 ?/. - c.*1697G>T r.(=) p.(=)
RNF121 NM_018320.4 ?/. - c.*5515C>A r.(=) p.(=)
IL18BP NM_173042.2 ?/. - c.554C>A r.(?) p.(Ser185Tyr)


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