rs851186

chr1-223132068-A-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003268.6(TLR5):c.-5+407T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.632 in 151,840 control chromosomes in the GnomAD database, including 30,896 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.63 (30896 hom., cov: 30)
• Consequence: TLR5 NM_003268.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.696

Genes affected

TLR5 (HGNC:11851): (toll like receptor 5) This gene encodes a member of the toll-like receptor (TLR) family, which plays a fundamental role in pathogen recognition and activation of innate immune responses. These receptors recognize distinct pathogen-associated molecular patterns that are expressed on infectious agents. The protein encoded by this gene recognizes bacterial flagellin, the principal component of bacterial flagella and a virulence factor. The activation of this receptor mobilizes the nuclear factor NF-kappaB, which in turn activates a host of inflammatory-related target genes. Mutations in this gene have been associated with both resistance and susceptibility to systemic lupus erythematosus, and susceptibility to Legionnaire disease.[provided by RefSeq, Dec 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.774 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TLR5	NM_003268.6	c.-5+407T>G		intron_variant		ENST00000642603.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TLR5	ENST00000642603.2	c.-5+407T>G		intron_variant			NM_003268.6	P1

Frequencies

GnomAD3 genomes AF: 0.632 AC: 95831 AN: 151718 Hom.: 30874 Cov.: 30

Gnomad AFR AF: 0.746

Gnomad AMI AF: 0.495

Gnomad AMR AF: 0.664

Gnomad ASJ AF: 0.595

Gnomad EAS AF: 0.794

Gnomad SAS AF: 0.574

Gnomad FIN AF: 0.507

Gnomad MID AF: 0.595

Gnomad NFE AF: 0.570

Gnomad OTH AF: 0.641

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.632 AC: 95904 AN: 151840 Hom.: 30896 Cov.: 30 AF XY: 0.629 AC XY: 46694 AN XY: 74200

Gnomad4 AFR AF: 0.746

Gnomad4 AMR AF: 0.664

Gnomad4 ASJ AF: 0.595

Gnomad4 EAS AF: 0.794

Gnomad4 SAS AF: 0.574

Gnomad4 FIN AF: 0.507

Gnomad4 NFE AF: 0.570

Gnomad4 OTH AF: 0.640

Alfa AF: 0.589 Hom.: 3323

Bravo AF: 0.651

Asia WGS AF: 0.693 AC: 2408 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
Cadd	Benign	7.0
Dann	Benign	0.92

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs851186; hg19: chr1-223305410; COSMIC: COSV60558343; COSMIC: COSV60558343;