NM_018291.5(FGGY):c.1334C>G (p.Ala445Gly) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Apr 25, 2023
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:: RCV004309589.1

Allele description [Variation Report for NM_018291.5(FGGY):c.1334C>G (p.Ala445Gly)]

NM_018291.5(FGGY):c.1334C>G (p.Ala445Gly)

Gene:

FGGY:FGGY carbohydrate kinase domain containing [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p32.1

Genomic location:

Preferred name:

NM_018291.5(FGGY):c.1334C>G (p.Ala445Gly)

HGVS:

NC_000001.11:g.59667320C>G
NG_030039.1:g.375368C>G
NM_001113411.2:c.1406C>G
NM_001244714.2:c.1070C>G
NM_001278224.2:c.437C>G
NM_001350790.2:c.1406C>G
NM_001350791.2:c.1334C>G
NM_001350792.2:c.1166C>G
NM_001350793.2:c.1166C>G
NM_001350794.2:c.1334C>G
NM_001350795.2:c.1142C>G
NM_001350796.2:c.998C>G
NM_001350797.2:c.932C>G
NM_001350798.2:c.1070C>G
NM_001350799.2:c.998C>G
NM_018291.5:c.1334C>GMANE SELECT
NP_001106882.1:p.Ala469Gly
NP_001231643.1:p.Ala357Gly
NP_001265153.1:p.Ala146Gly
NP_001337719.1:p.Ala469Gly
NP_001337720.1:p.Ala445Gly
NP_001337721.1:p.Ala389Gly
NP_001337722.1:p.Ala389Gly
NP_001337723.1:p.Ala445Gly
NP_001337724.1:p.Ala381Gly
NP_001337725.1:p.Ala333Gly
NP_001337726.1:p.Ala311Gly
NP_001337727.1:p.Ala357Gly
NP_001337728.1:p.Ala333Gly
NP_060761.3:p.Ala445Gly
NC_000001.10:g.60132992C>G
NM_001113411.1:c.1406C>G
NR_103473.2:n.1422C>G

Protein change:

A146G

Molecular consequence:

NM_001113411.2:c.1406C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001244714.2:c.1070C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001278224.2:c.437C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350790.2:c.1406C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350791.2:c.1334C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350792.2:c.1166C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350793.2:c.1166C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350794.2:c.1334C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350795.2:c.1142C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350796.2:c.998C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350797.2:c.932C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350798.2:c.1070C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350799.2:c.998C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_018291.5:c.1334C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_103473.2:n.1422C>G - 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
SCV003969946	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Apr 25, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003969946

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Apr 25, 2023)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003969946.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.1406C>G (p.A469G) alteration is located in exon 14 (coding exon 13) of the FGGY gene. This alteration results from a C to G substitution at nucleotide position 1406, causing the alanine (A) at amino acid position 469 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 10, 2024

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