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NM_000548.5(TSC2):c.4850C>A (p.Ala1617Asp) AND Tuberous sclerosis 2

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 13, 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:
RCV002300532.4

Allele description [Variation Report for NM_000548.5(TSC2):c.4850C>A (p.Ala1617Asp)]

NM_000548.5(TSC2):c.4850C>A (p.Ala1617Asp)

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.4850C>A (p.Ala1617Asp)
HGVS:
  • NC_000016.10:g.2086732C>A
  • NG_005895.1:g.42427C>A
  • NG_008617.1:g.56489G>T
  • NM_000548.5:c.4850C>AMANE SELECT
  • NM_001077183.3:c.4649C>A
  • NM_001114382.3:c.4781C>A
  • NM_001318827.2:c.4541C>A
  • NM_001318829.2:c.4505C>A
  • NM_001318831.2:c.4118C>A
  • NM_001318832.2:c.4682C>A
  • NM_001363528.2:c.4652C>A
  • NM_001370404.1:c.4718C>A
  • NM_001370405.1:c.4721C>A
  • NM_001406663.1:c.4847C>A
  • NM_001406664.1:c.4778C>A
  • NM_001406665.1:c.4772C>A
  • NM_001406667.1:c.4742C>A
  • NM_001406668.1:c.4739C>A
  • NM_001406670.1:c.4670C>A
  • NM_001406671.1:c.4640C>A
  • NM_001406673.1:c.4637C>A
  • NM_001406675.1:c.4634C>A
  • NM_001406676.1:c.4631C>A
  • NM_001406677.1:c.4592C>A
  • NM_001406678.1:c.4538C>A
  • NM_001406679.1:c.4502C>A
  • NM_001406680.1:c.4250C>A
  • NM_001406681.1:c.4190C>A
  • NM_001406682.1:c.4181C>A
  • NM_001406683.1:c.4181C>A
  • NM_001406684.1:c.4178C>A
  • NM_001406685.1:c.4052C>A
  • NM_001406686.1:c.4052C>A
  • NM_001406687.1:c.4049C>A
  • NM_001406688.1:c.4049C>A
  • NM_001406689.1:c.3437C>A
  • NM_001406690.1:c.3377C>A
  • NM_001406691.1:c.3374C>A
  • NM_001406692.1:c.3308C>A
  • NM_001406693.1:c.3308C>A
  • NM_001406694.1:c.3308C>A
  • NM_001406695.1:c.3305C>A
  • NM_001406696.1:c.3305C>A
  • NM_001406697.1:c.3305C>A
  • NM_001406698.1:c.3047C>A
  • NM_021055.3:c.4721C>A
  • NP_000539.2:p.Ala1617Asp
  • NP_000539.2:p.Ala1617Asp
  • NP_001070651.1:p.Ala1550Asp
  • NP_001107854.1:p.Ala1594Asp
  • NP_001305756.1:p.Ala1514Asp
  • NP_001305758.1:p.Ala1502Asp
  • NP_001305760.1:p.Ala1373Asp
  • NP_001305761.1:p.Ala1561Asp
  • NP_001350457.1:p.Ala1551Asp
  • NP_001357333.1:p.Ala1573Asp
  • NP_001357334.1:p.Ala1574Asp
  • NP_001393592.1:p.Ala1616Asp
  • NP_001393593.1:p.Ala1593Asp
  • NP_001393594.1:p.Ala1591Asp
  • NP_001393596.1:p.Ala1581Asp
  • NP_001393597.1:p.Ala1580Asp
  • NP_001393599.1:p.Ala1557Asp
  • NP_001393600.1:p.Ala1547Asp
  • NP_001393602.1:p.Ala1546Asp
  • NP_001393604.1:p.Ala1545Asp
  • NP_001393605.1:p.Ala1544Asp
  • NP_001393606.1:p.Ala1531Asp
  • NP_001393607.1:p.Ala1513Asp
  • NP_001393608.1:p.Ala1501Asp
  • NP_001393609.1:p.Ala1417Asp
  • NP_001393610.1:p.Ala1397Asp
  • NP_001393611.1:p.Ala1394Asp
  • NP_001393612.1:p.Ala1394Asp
  • NP_001393613.1:p.Ala1393Asp
  • NP_001393614.1:p.Ala1351Asp
  • NP_001393615.1:p.Ala1351Asp
  • NP_001393616.1:p.Ala1350Asp
  • NP_001393617.1:p.Ala1350Asp
  • NP_001393618.1:p.Ala1146Asp
  • NP_001393619.1:p.Ala1126Asp
  • NP_001393620.1:p.Ala1125Asp
  • NP_001393621.1:p.Ala1103Asp
  • NP_001393622.1:p.Ala1103Asp
  • NP_001393623.1:p.Ala1103Asp
  • NP_001393624.1:p.Ala1102Asp
  • NP_001393625.1:p.Ala1102Asp
  • NP_001393626.1:p.Ala1102Asp
  • NP_001393627.1:p.Ala1016Asp
  • NP_066399.2:p.Ala1574Asp
  • LRG_487t1:c.4850C>A
  • LRG_487:g.42427C>A
  • LRG_487p1:p.Ala1617Asp
  • NC_000016.9:g.2136733C>A
  • NM_000548.3:c.4850C>A
  • NR_176225.1:n.4802C>A
  • NR_176226.1:n.5050C>A
  • NR_176227.1:n.4978C>A
  • NR_176228.1:n.4799C>A
Protein change:
A1016D
Molecular consequence:
  • NM_000548.5:c.4850C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001077183.3:c.4649C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001114382.3:c.4781C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001318827.2:c.4541C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001318829.2:c.4505C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001318831.2:c.4118C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001318832.2:c.4682C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001363528.2:c.4652C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370404.1:c.4718C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370405.1:c.4721C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406663.1:c.4847C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406664.1:c.4778C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406665.1:c.4772C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406667.1:c.4742C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406668.1:c.4739C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406670.1:c.4670C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406671.1:c.4640C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406673.1:c.4637C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406675.1:c.4634C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406676.1:c.4631C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406677.1:c.4592C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406678.1:c.4538C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406679.1:c.4502C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406680.1:c.4250C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406681.1:c.4190C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406682.1:c.4181C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406683.1:c.4181C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406684.1:c.4178C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406685.1:c.4052C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406686.1:c.4052C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406687.1:c.4049C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406688.1:c.4049C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406689.1:c.3437C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406690.1:c.3377C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406691.1:c.3374C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406692.1:c.3308C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406693.1:c.3308C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406694.1:c.3308C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406695.1:c.3305C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406696.1:c.3305C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406697.1:c.3305C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406698.1:c.3047C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_021055.3:c.4721C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

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

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002594322Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Oct 13, 2022) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical 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, SCV002594322.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical 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. 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: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals affected with TSC2-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces alanine, which is neutral and non-polar, with aspartic acid, which is acidic and polar, at codon 1617 of the TSC2 protein (p.Ala1617Asp).

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024