Variant #0000609165 (NC_000004.11:g.187003729C>G, NM_003265.2:c.889C>G (TLR3))

Chromosome 4
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.187003729C>G
DNA change (hg38) g.186082575C>G
Published as TLR3(NM_003265.2):c.889C>G (p.L297V), TLR3(NM_003265.3):c.889C>G (p.L297V)
ISCN -
DB-ID TLR3_000011 See all 4 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) 0.00152 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TLR3 NM_003265.2 ?/. - c.889C>G r.(?) p.(Leu297Val)


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