NM_018344.6(SLC29A3):c.902T>A (p.Ile301Asn) AND H syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 26, 2021
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:: RCV001914889.5

Allele description [Variation Report for NM_018344.6(SLC29A3):c.902T>A (p.Ile301Asn)]

NM_018344.6(SLC29A3):c.902T>A (p.Ile301Asn)

Gene:

SLC29A3:solute carrier family 29 member 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q22.1

Genomic location:

Preferred name:

NM_018344.6(SLC29A3):c.902T>A (p.Ile301Asn)

HGVS:

NC_000010.11:g.71362082T>A
NG_017066.2:g.47824T>A
NM_001174098.2:c.*131T>A
NM_001363518.2:c.668T>A
NM_018344.6:c.902T>AMANE SELECT
NP_001350447.1:p.Ile223Asn
NP_060814.4:p.Ile301Asn
LRG_1318t1:c.902T>A
LRG_1318:g.47824T>A
LRG_1318p1:p.Ile301Asn
NC_000010.10:g.73121839T>A
NR_033413.2:n.870T>A
NR_033414.2:n.643T>A

Protein change:

I223N

Links:

dbSNP: rs1307741029

NCBI 1000 Genomes Browser:

rs1307741029

Molecular consequence:

NM_001174098.2:c.*131T>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001363518.2:c.668T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_018344.6:c.902T>A - missense variant - [Sequence Ontology: SO:0001583]
NR_033413.2:n.870T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_033414.2:n.643T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: H syndrome
Synonyms:: Histiocytosis with joint contractures and sensorineural deafness; Faisalabad histiocytosis; HISTIOCYTOSIS AND LYMPHADENOPATHY WITH OR WITHOUT CUTANEOUS, CARDIAC, AND/OR ENDOCRINE FEATURES, JOINT CONTRACTURES, AND/OR DEAFNESS; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0011273; MedGen: C1864445; Orphanet: 168569; OMIM: 602782

Recent activity

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yu20h04.s1 Soares fetal liver spleen 1NFLS Homo sapiens cDNA clone IMAGE:234391 ...
yu20h04.s1 Soares fetal liver spleen 1NFLS Homo sapiens cDNA clone IMAGE:234391 3', mRNA sequence
gi|1102913|gnl|dbEST|399514|gb|H952

Nucleotide
Polygonum toktogulicum voucher FRU:Lazkov s/n internal transcribed spacer 1, 5.8...
Polygonum toktogulicum voucher FRU:Lazkov s/n internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence
gi|284811171|gb|GQ340057.1|

Nucleotide
bone morphogenetic protein 7b isoform X3 [Acanthopagrus latus]
bone morphogenetic protein 7b isoform X3 [Acanthopagrus latus]
gi|2642094917|gb|WQY91215.1|

Protein
Related DataSets for GEO Profiles (Select 44326282) (1)
GEO DataSets
Rheumatoid arthritis and osteoarthritis: synovial fibroblasts
Rheumatoid arthritis and osteoarthritis: synovial fibroblasts
Accession: GDS2931

GEO DataSets

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002145763	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Aug 26, 2021)	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

SCV002145763

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Aug 26, 2021)

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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV002145763.2

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

Description

This sequence change replaces isoleucine with asparagine at codon 301 of the SLC29A3 protein (p.Ile301Asn). The isoleucine residue is highly conserved and there is a large physicochemical difference between isoleucine and asparagine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with SLC29A3-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

#	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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