Variant #0000611831 (NC_000009.11:g.120476694G>A, NM_138554.4:c.2288G>A (TLR4))

Chromosome 9
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.120476694G>A
DNA change (hg38) g.117714416G>A
Published as TLR4(NM_003266.3):c.2168G>A (p.R723H), TLR4(NM_138554.3):c.2288G>A (p.R763H)
ISCN -
DB-ID TLR4_000010 See all 2 reported entries
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) 0.00119 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TLR4 NM_138554.4 -?/. - c.2288G>A r.(?) p.(Arg763His)


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