NM_000264.5(PTCH1):c.3364A>G (p.Met1122Val) AND Gorlin syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 11, 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:: RCV001344306.7

Allele description [Variation Report for NM_000264.5(PTCH1):c.3364A>G (p.Met1122Val)]

NM_000264.5(PTCH1):c.3364A>G (p.Met1122Val)

Gene:

PTCH1:patched 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q22.32

Genomic location:

Preferred name:

NM_000264.5(PTCH1):c.3364A>G (p.Met1122Val)

HGVS:

NC_000009.12:g.95453563T>C
NG_007664.1:g.68403A>G
NM_000264.3:c.3364A>G
NM_000264.5:c.3364A>GMANE SELECT
NM_001083602.3:c.3166A>G
NM_001083603.3:c.3361A>G
NM_001083604.3:c.2911A>G
NM_001083605.3:c.2911A>G
NM_001083606.3:c.2911A>G
NM_001083607.3:c.2911A>G
NM_001354918.2:c.3208A>G
NP_000255.2:p.Met1122Val
NP_001077071.1:p.Met1056Val
NP_001077072.1:p.Met1121Val
NP_001077073.1:p.Met971Val
NP_001077074.1:p.Met971Val
NP_001077075.1:p.Met971Val
NP_001077076.1:p.Met971Val
NP_001341847.1:p.Met1070Val
LRG_515t1:c.3364A>G
LRG_515:g.68403A>G
NC_000009.11:g.98215845T>C
NR_149061.2:n.4103A>G

Protein change:

M1056V

Links:

dbSNP: rs1838661361

NCBI 1000 Genomes Browser:

rs1838661361

Molecular consequence:

NM_000264.5:c.3364A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001083602.3:c.3166A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001083603.3:c.3361A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001083604.3:c.2911A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001083605.3:c.2911A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001083606.3:c.2911A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001083607.3:c.2911A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001354918.2:c.3208A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_149061.2:n.4103A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Gorlin syndrome
Synonyms:: Basal cell nevus syndrome
Identifiers:: MONDO: MONDO:0007187; MedGen: C0004779; Orphanet: 377; OMIM: PS109400

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001538348	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jul 11, 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

SCV001538348

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jul 11, 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, SCV001538348.5

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

Description

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. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt PTCH1 protein function. ClinVar contains an entry for this variant (Variation ID: 1040630). This variant has not been reported in the literature in individuals affected with PTCH1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces methionine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 1122 of the PTCH1 protein (p.Met1122Val).

#	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

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