NM_004130.4(GYG1):c.601T>G (p.Phe201Val) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 5, 2022
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:: RCV002563564.2

Allele description [Variation Report for NM_004130.4(GYG1):c.601T>G (p.Phe201Val)]

NM_004130.4(GYG1):c.601T>G (p.Phe201Val)

Gene:

GYG1:glycogenin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3q24

Genomic location:

Preferred name:

NM_004130.4(GYG1):c.601T>G (p.Phe201Val)

HGVS:

NC_000003.12:g.149009395T>G
NG_027677.1:g.22988T>G
NM_001184720.2:c.601T>G
NM_001184721.2:c.601T>G
NM_004130.3:c.601T>G
NM_004130.4:c.601T>GMANE SELECT
NP_001171649.1:p.Phe201Val
NP_001171650.1:p.Phe201Val
NP_004121.2:p.Phe201Val
NC_000003.11:g.148727182T>G

Protein change:

F201V

Links:

dbSNP: rs142318183

NCBI 1000 Genomes Browser:

rs142318183

Molecular consequence:

NM_001184720.2:c.601T>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001184721.2:c.601T>G - missense variant - [Sequence Ontology: SO:0001583]
NM_004130.4:c.601T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

Recent activity

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Mus musculus solute carrier family 7 (cationic amino acid transporter, y+ system...
Mus musculus solute carrier family 7 (cationic amino acid transporter, y+ system), member 4 (Slc7a4), transcript variant 3, mRNA
gi|2449300206|ref|NM_001359891.2|

Nucleotide
PREDICTED: Homo sapiens phosphatidylinositol 4-kinase beta (PI4KB), transcript v...
PREDICTED: Homo sapiens phosphatidylinositol 4-kinase beta (PI4KB), transcript variant X6, mRNA
gi|2462510155|ref|XM_054337070.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003671645	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 5, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003671645

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 5, 2022)

germline

clinical testing

Citation Link

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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, SCV003671645.2

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

Description

The c.601T>G (p.F201V) alteration is located in exon 5 (coding exon 5) of the GYG1 gene. This alteration results from a T to G substitution at nucleotide position 601, causing the phenylalanine (F) at amino acid position 201 to be replaced by a valine (V). 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: Sep 29, 2024

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