NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met) AND not specified

Clinical significance:Likely benign (Last evaluated: Mar 22, 2021)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001662639.1

Allele description [Variation Report for NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met)]

NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met)

Gene:
TTN:titin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met)
HGVS:
  • NC_000002.12:g.178712437G>A
  • NG_011618.3:g.123366C>T
  • NM_001256850.1:c.26534C>T
  • NM_001267550.2:c.27485C>TMANE SELECT
  • NM_003319.4:c.13282+25645C>T
  • NM_133378.4:c.23753C>T
  • NM_133432.3:c.13657+25645C>T
  • NM_133437.4:c.13858+25645C>T
  • NP_001243779.1:p.Thr8845Met
  • NP_001254479.2:p.Thr9162Met
  • NP_596869.4:p.Thr7918Met
  • LRG_391:g.123366C>T
  • NC_000002.11:g.179577164G>A
  • NM_001267550.1:c.27485C>T
Protein change:
T7918M
Links:
dbSNP: rs199793620
NCBI 1000 Genomes Browser:
rs199793620
Molecular consequence:
  • NM_003319.4:c.13282+25645C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133432.3:c.13657+25645C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133437.4:c.13858+25645C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001256850.1:c.26534C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001267550.2:c.27485C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133378.4:c.23753C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001880238Athena Diagnostics Inccriteria provided, single submitter
Likely benign
(Mar 22, 2021)
unknownclinical testing

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

Summary from all submissions

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

Citations

PubMed

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.

Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.

Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.

PubMed [citation]
PMID:
26467025
PMCID:
PMC4737317

Details of each submission

From Athena Diagnostics Inc, SCV001880238.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 27, 2021

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