NM_144596.4(TTC8):c.466G>A (p.Gly156Arg) AND Bardet-Biedl syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 19, 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:: RCV001367225.4

Allele description [Variation Report for NM_144596.4(TTC8):c.466G>A (p.Gly156Arg)]

NM_144596.4(TTC8):c.466G>A (p.Gly156Arg)

Gene:

TTC8:tetratricopeptide repeat domain 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q31.3

Genomic location:

Preferred name:

NM_144596.4(TTC8):c.466G>A (p.Gly156Arg)

HGVS:

NC_000014.9:g.88841173G>A
NG_008126.2:g.22021G>A
NM_001288781.1:c.436G>A
NM_001288782.1:c.-127G>A
NM_001288783.1:c.-222G>A
NM_001366535.2:c.436G>A
NM_001366536.2:c.436G>A
NM_144596.3:c.466G>A
NM_144596.4:c.466G>AMANE SELECT
NM_198309.3:c.436G>A
NM_198310.3:c.436G>A
NP_001275710.1:p.Gly146Arg
NP_001353464.1:p.Gly146Arg
NP_001353465.1:p.Gly146Arg
NP_653197.2:p.Gly156Arg
NP_938051.1:p.Gly146Arg
NP_938052.1:p.Gly146Arg
NC_000014.8:g.89307517G>A
NM_198309.2:c.436G>A
NR_159362.2:n.493G>A

Protein change:

G146R

Links:

dbSNP: rs750521601

NCBI 1000 Genomes Browser:

rs750521601

Molecular consequence:

NM_001288782.1:c.-127G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001288783.1:c.-222G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001288781.1:c.436G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001366535.2:c.436G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001366536.2:c.436G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_144596.4:c.466G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_198309.3:c.436G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_198310.3:c.436G>A - missense variant - [Sequence Ontology: SO:0001583]
NR_159362.2:n.493G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Bardet-Biedl syndrome (BBS)
Identifiers:: MONDO: MONDO:0015229; MedGen: C0752166; Orphanet: 110; OMIM: PS209900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001563570	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Aug 19, 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

SCV001563570

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Aug 19, 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, SCV001563570.3

#	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 glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 146 of the TTC8 protein (p.Gly146Arg). This variant is present in population databases (rs750521601, gnomAD 0.03%). This variant has not been reported in the literature in individuals affected with TTC8-related conditions. ClinVar contains an entry for this variant (Variation ID: 1058128). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). 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.

#	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: Oct 13, 2024

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