NM_182919.4(TICAM1):c.1355T>C (p.Ile452Thr) AND Herpes simplex encephalitis, susceptibility to, 4

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 7, 2022
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001347067.5

Allele description [Variation Report for NM_182919.4(TICAM1):c.1355T>C (p.Ile452Thr)]

NM_182919.4(TICAM1):c.1355T>C (p.Ile452Thr)

Gene:

TICAM1:TIR domain containing adaptor molecule 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.3

Genomic location:

Preferred name:

NM_182919.4(TICAM1):c.1355T>C (p.Ile452Thr)

HGVS:

NC_000019.10:g.4817023A>G
NG_031998.1:g.19720T>C
NM_001385678.1:c.1313T>C
NM_001385679.1:c.1220T>C
NM_001385680.1:c.713T>C
NM_182919.4:c.1355T>CMANE SELECT
NP_001372607.1:p.Ile438Thr
NP_001372608.1:p.Ile407Thr
NP_001372609.1:p.Ile238Thr
NP_891549.1:p.Ile452Thr
LRG_358:g.19720T>C
NC_000019.9:g.4817035A>G

Protein change:

I238T

Links:

dbSNP: rs770034965

NCBI 1000 Genomes Browser:

rs770034965

Molecular consequence:

NM_001385678.1:c.1313T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001385679.1:c.1220T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001385680.1:c.713T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_182919.4:c.1355T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Herpes simplex encephalitis, susceptibility to, 4 (IIAE6)
Synonyms:: ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6
Identifiers:: MONDO: MONDO:0013921; MedGen: C3553869; Orphanet: 1930; OMIM: 614850

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001541308	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Sep 7, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001541308

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Sep 7, 2022)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001541308.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

This sequence change replaces isoleucine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 452 of the TICAM1 protein (p.Ile452Thr). This variant is present in population databases (no rsID available, gnomAD no frequency). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The threonine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. ClinVar contains an entry for this variant (Variation ID: 1043022). This variant has not been reported in the literature in individuals affected with TICAM1-related conditions.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine