NM_001080432.3(FTO):c.601G>A (p.Val201Ile) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 29, 2020
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:: RCV002558147.2

Allele description [Variation Report for NM_001080432.3(FTO):c.601G>A (p.Val201Ile)]

NM_001080432.3(FTO):c.601G>A (p.Val201Ile)

Gene:

FTO:FTO alpha-ketoglutarate dependent dioxygenase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q12.2

Genomic location:

Preferred name:

NM_001080432.3(FTO):c.601G>A (p.Val201Ile)

HGVS:

NC_000016.10:g.53826341G>A
NG_012969.1:g.127379G>A
NM_001080432.3:c.601G>AMANE SELECT
NM_001363891.1:c.601G>A
NM_001363894.1:c.601G>A
NM_001363896.1:c.601G>A
NM_001363897.1:c.523G>A
NM_001363898.1:c.601G>A
NM_001363899.1:c.601G>A
NM_001363900.1:c.601G>A
NM_001363901.1:c.601G>A
NM_001363903.1:c.601G>A
NM_001363905.1:c.88G>A
NM_001363988.1:c.601G>A
NP_001073901.1:p.Val201Ile
NP_001350820.1:p.Val201Ile
NP_001350823.1:p.Val201Ile
NP_001350825.1:p.Val201Ile
NP_001350826.1:p.Val175Ile
NP_001350827.1:p.Val201Ile
NP_001350828.1:p.Val201Ile
NP_001350829.1:p.Val201Ile
NP_001350830.1:p.Val201Ile
NP_001350832.1:p.Val201Ile
NP_001350834.1:p.Val30Ile
NP_001350917.1:p.Val201Ile
NC_000016.9:g.53860253G>A
NC_000016.9:g.53860253G>A
NM_001080432.2:c.601G>A

Protein change:

V175I

Links:

dbSNP: rs150450891

NCBI 1000 Genomes Browser:

rs150450891

Molecular consequence:

NM_001080432.3:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363891.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363894.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363896.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363897.1:c.523G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363898.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363899.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363900.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363901.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363903.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363905.1:c.88G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363988.1:c.601G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

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

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003643736	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 29, 2020)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003643736

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 29, 2020)

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, SCV003643736.2

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

Description

The c.601G>A (p.V201I) alteration is located in exon 3 (coding exon 3) of the FTO gene. This alteration results from a G to A substitution at nucleotide position 601, causing the valine (V) at amino acid position 201 to be replaced by an isoleucine (I). The p.V201I alteration is predicted to be tolerated by in silico analysis. 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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