NM_001079802.2(FKTN):c.508G>A (p.Ala170Thr) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 28, 2017
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:: RCV000502129.6

Allele description [Variation Report for NM_001079802.2(FKTN):c.508G>A (p.Ala170Thr)]

NM_001079802.2(FKTN):c.508G>A (p.Ala170Thr)

Gene:

FKTN:fukutin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q31.2

Genomic location:

Preferred name:

NM_001079802.2(FKTN):c.508G>A (p.Ala170Thr)

HGVS:

NC_000009.12:g.105604353G>A
NG_008754.1:g.51224G>A
NM_001079802.2:c.508G>AMANE SELECT
NM_001198963.2:c.508G>A
NM_001351496.2:c.508G>A
NM_001351497.2:c.439G>A
NM_001351498.2:c.508G>A
NM_001351499.2:c.112G>A
NM_001351500.2:c.112G>A
NM_001351501.2:c.112G>A
NM_001351502.2:c.112G>A
NM_006731.2:c.508G>A
NP_001073270.1:p.Ala170Thr
NP_001073270.1:p.Ala170Thr
NP_001185892.1:p.Ala170Thr
NP_001338425.1:p.Ala170Thr
NP_001338426.1:p.Ala147Thr
NP_001338427.1:p.Ala170Thr
NP_001338428.1:p.Ala38Thr
NP_001338429.1:p.Ala38Thr
NP_001338430.1:p.Ala38Thr
NP_001338431.1:p.Ala38Thr
NP_006722.2:p.Ala170Thr
LRG_434t1:c.508G>A
LRG_434t2:c.508G>A
LRG_434:g.51224G>A
LRG_434p1:p.Ala170Thr
LRG_434p2:p.Ala170Thr
NC_000009.11:g.108366634G>A
NM_001079802.1:c.508G>A
NR_147213.2:n.723G>A
NR_147214.2:n.631G>A

Protein change:

A147T

Links:

dbSNP: rs778818366

NCBI 1000 Genomes Browser:

rs778818366

Molecular consequence:

NM_001079802.2:c.508G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001198963.2:c.508G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001351496.2:c.508G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001351497.2:c.439G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001351498.2:c.508G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001351499.2:c.112G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001351500.2:c.112G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001351501.2:c.112G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001351502.2:c.112G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_006731.2:c.508G>A - missense variant - [Sequence Ontology: SO:0001583]
NR_147213.2:n.723G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_147214.2:n.631G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000594790	Genetic Services Laboratory, University of Chicago	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Feb 28, 2017)	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

SCV000594790

Genetic Services Laboratory, University of Chicago

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Feb 28, 2017)

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

Citations

PubMed

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 Genetic Services Laboratory, University of Chicago, SCV000594790.1

#	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: Sep 29, 2024

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