U.S. flag

An official website of the United States government

NM_000368.5(TSC1):c.853T>G (p.Phe285Val) AND not provided

Germline classification:
Benign (1 submission)
Last evaluated:
Oct 8, 2020
Review status:
criteria provided, conflicting classifications
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:
RCV001618239.6

Allele description [Variation Report for NM_000368.5(TSC1):c.853T>G (p.Phe285Val)]

NM_000368.5(TSC1):c.853T>G (p.Phe285Val)

Gene:
TSC1:TSC complex subunit 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q34.13
Genomic location:
Preferred name:
NM_000368.5(TSC1):c.853T>G (p.Phe285Val)
HGVS:
  • NC_000009.12:g.132912342A>C
  • NG_012386.1:g.37292T>G
  • NM_000368.5:c.853T>GMANE SELECT
  • NM_001162426.2:c.853T>G
  • NM_001162427.2:c.700T>G
  • NM_001362177.2:c.490T>G
  • NP_000359.1:p.Phe285Val
  • NP_000359.1:p.Phe285Val
  • NP_001155898.1:p.Phe285Val
  • NP_001155899.1:p.Phe234Val
  • NP_001349106.1:p.Phe164Val
  • LRG_486t1:c.853T>G
  • LRG_486:g.37292T>G
  • LRG_486p1:p.Phe285Val
  • NC_000009.11:g.135787729A>C
  • NM_000368.4:c.853T>G
  • p.(Phe285Val)
Protein change:
F164V
Links:
Tuberous sclerosis database (TSC1): TSC1_00509; dbSNP: rs377076733
NCBI 1000 Genomes Browser:
rs377076733
Molecular consequence:
  • NM_000368.5:c.853T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001162426.2:c.853T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001162427.2:c.700T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001362177.2:c.490T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001847640GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Benign
(Oct 8, 2020)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV001847640.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant is associated with the following publications: (PMID: 24728327, 23401075, 21309039)

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

Last Updated: Sep 29, 2024