NM_000548.5(TSC2):c.5338A>C (p.Thr1780Pro) AND Tuberous sclerosis 2

Germline classification:: Benign (2 submissions)
Last evaluated:: Dec 14, 2023
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000548829.13

Allele description [Variation Report for NM_000548.5(TSC2):c.5338A>C (p.Thr1780Pro)]

NM_000548.5(TSC2):c.5338A>C (p.Thr1780Pro)

Gene:

TSC2:TSC complex subunit 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16p13.3

Genomic location:

Preferred name:

NM_000548.5(TSC2):c.5338A>C (p.Thr1780Pro)

HGVS:

NC_000016.10:g.2088524A>C
NG_005895.1:g.44219A>C
NG_008617.1:g.54697T>G
NM_000548.5:c.5338A>CMANE SELECT
NM_001077183.3:c.5137A>C
NM_001114382.3:c.5269A>C
NM_001318827.2:c.5029A>C
NM_001318829.2:c.4993A>C
NM_001318831.2:c.4606A>C
NM_001318832.2:c.5170A>C
NM_001363528.2:c.5140A>C
NM_001370404.1:c.5206A>C
NM_001370405.1:c.5197A>C
NM_021055.3:c.5209A>C
NP_000539.2:p.Thr1780Pro
NP_001070651.1:p.Thr1713Pro
NP_001107854.1:p.Thr1757Pro
NP_001305756.1:p.Thr1677Pro
NP_001305758.1:p.Thr1665Pro
NP_001305760.1:p.Thr1536Pro
NP_001305761.1:p.Thr1724Pro
NP_001350457.1:p.Thr1714Pro
NP_001357333.1:p.Thr1736Pro
NP_001357334.1:p.Thr1733Pro
NP_066399.2:p.Thr1737Pro
LRG_487t1:c.5338A>C
LRG_487:g.44219A>C
NC_000016.9:g.2138525A>C
NM_000548.3:c.5338A>C
NM_000548.4:c.5338A>C

Protein change:

T1536P

Links:

dbSNP: rs989487316

NCBI 1000 Genomes Browser:

rs989487316

Molecular consequence:

NM_000548.5:c.5338A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001077183.3:c.5137A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001114382.3:c.5269A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318827.2:c.5029A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318829.2:c.4993A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318831.2:c.4606A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318832.2:c.5170A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001363528.2:c.5140A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001370404.1:c.5206A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001370405.1:c.5197A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_021055.3:c.5209A>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Tuberous sclerosis 2 (TSC2)
Identifiers:: MONDO: MONDO:0013199; MedGen: C1860707; Orphanet: 805; OMIM: 613254

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000644635	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Benign (Dec 14, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002039955	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Nov 7, 2021)	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

SCV000644635

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Benign
(Dec 14, 2023)

germline

clinical testing

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

SCV002039955

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Nov 7, 2021)

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	no	not provided	not provided	not provided	not provided	not provided	clinical testing
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

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000644635.8

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

#	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

From Genome-Nilou Lab, SCV002039955.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Oct 13, 2024

ClinVar

Relating variation to medicine