Variant #0000895921 (NC_000023.10:g.12904970C>T, TLR7(NM_016562.3):c.1343C>T)

Chromosome X
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.12904970C>T
DNA change (hg38) -
Published as TLR7(NM_016562.3):c.1343C>T (p.(Ala448Val)), TLR7(NM_016562.4):c.1343C>T (p.A448V)
ISCN -
DB-ID TLR7_000004 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) 0.0029 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TLR7 NM_016562.3 -?/. - c.1343C>T r.(?) p.(Ala448Val)