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NM_001079802.2(FKTN):c.681G>A (p.Leu227=) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 21, 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:
RCV000725721.6

Allele description [Variation Report for NM_001079802.2(FKTN):c.681G>A (p.Leu227=)]

NM_001079802.2(FKTN):c.681G>A (p.Leu227=)

Gene:
FKTN:fukutin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q31.2
Genomic location:
Preferred name:
NM_001079802.2(FKTN):c.681G>A (p.Leu227=)
HGVS:
  • NC_000009.12:g.105607852G>A
  • NG_008754.1:g.54723G>A
  • NM_001079802.2:c.681G>AMANE SELECT
  • NM_001198963.2:c.681G>A
  • NM_001351496.2:c.681G>A
  • NM_001351497.2:c.612G>A
  • NM_001351498.2:c.681G>A
  • NM_001351499.2:c.285G>A
  • NM_001351500.2:c.285G>A
  • NM_001351501.2:c.285G>A
  • NM_001351502.2:c.285G>A
  • NM_006731.2:c.681G>A
  • NP_001073270.1:p.Leu227=
  • NP_001073270.1:p.Leu227=
  • NP_001185892.1:p.Leu227=
  • NP_001338425.1:p.Leu227=
  • NP_001338426.1:p.Leu204=
  • NP_001338427.1:p.Leu227=
  • NP_001338428.1:p.Leu95=
  • NP_001338429.1:p.Leu95=
  • NP_001338430.1:p.Leu95=
  • NP_001338431.1:p.Leu95=
  • NP_006722.2:p.Leu227=
  • LRG_434t1:c.681G>A
  • LRG_434t2:c.681G>A
  • LRG_434:g.54723G>A
  • LRG_434p1:p.Leu227=
  • LRG_434p2:p.Leu227=
  • NC_000009.11:g.108370133G>A
  • NM_001079802.1:c.681G>A
  • NR_147213.2:n.896G>A
  • NR_147214.2:n.804G>A
Links:
dbSNP: rs142604625
NCBI 1000 Genomes Browser:
rs142604625
Molecular consequence:
  • NR_147213.2:n.896G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_147214.2:n.804G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_001079802.2:c.681G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001198963.2:c.681G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001351496.2:c.681G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001351497.2:c.612G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001351498.2:c.681G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001351499.2:c.285G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001351500.2:c.285G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001351501.2:c.285G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001351502.2:c.285G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_006731.2:c.681G>A - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
9

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000338849Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL Classification Definitions 2015)
Uncertain significance
(Nov 21, 2017)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown9not providednot providednot providednot providedclinical testing

Details of each submission

From Eurofins Ntd Llc (ga), SCV000338849.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided9not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided9not providednot providednot provided

Last Updated: Sep 29, 2024