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NM_002206.3(ITGA7):c.1396G>A (p.Ala466Thr) AND Congenital muscular dystrophy due to integrin alpha-7 deficiency

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Jun 1, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000703797.9

Allele description [Variation Report for NM_002206.3(ITGA7):c.1396G>A (p.Ala466Thr)]

NM_002206.3(ITGA7):c.1396G>A (p.Ala466Thr)

Gene:
ITGA7:integrin subunit alpha 7 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
12q13.2
Genomic location:
Preferred name:
NM_002206.3(ITGA7):c.1396G>A (p.Ala466Thr)
HGVS:
  • NC_000012.12:g.55697708C>T
  • NG_012343.1:g.19598G>A
  • NM_001144996.2:c.1408G>A
  • NM_001144997.2:c.1117G>A
  • NM_001367993.1:c.1069G>A
  • NM_001367994.1:c.52G>A
  • NM_001374465.1:c.1396G>A
  • NM_001410977.1:c.1528G>A
  • NM_001414029.1:c.1408G>A
  • NM_001414030.1:c.1321G>A
  • NM_001414031.1:c.1309G>A
  • NM_001414032.1:c.1276G>A
  • NM_001414033.1:c.1213G>A
  • NM_001414034.1:c.1396G>A
  • NM_001414035.1:c.1057G>A
  • NM_002206.3:c.1396G>AMANE SELECT
  • NP_001138468.1:p.Ala470Thr
  • NP_001138469.1:p.Ala373Thr
  • NP_001138469.1:p.Ala373Thr
  • NP_001354922.1:p.Ala357Thr
  • NP_001354923.1:p.Ala18Thr
  • NP_001361394.1:p.Ala466Thr
  • NP_001397906.1:p.Ala510Thr
  • NP_001400958.1:p.Ala470Thr
  • NP_001400959.1:p.Ala441Thr
  • NP_001400960.1:p.Ala437Thr
  • NP_001400961.1:p.Ala426Thr
  • NP_001400962.1:p.Ala405Thr
  • NP_001400963.1:p.Ala466Thr
  • NP_001400964.1:p.Ala353Thr
  • NP_002197.2:p.Ala466Thr
  • LRG_871t1:c.1396G>A
  • LRG_871t2:c.1117G>A
  • LRG_871:g.19598G>A
  • LRG_871p1:p.Ala466Thr
  • LRG_871p2:p.Ala373Thr
  • NC_000012.11:g.56091492C>T
  • NM_001144997.1:c.1117G>A
  • NM_002206.2:c.1396G>A
Protein change:
A18T
Links:
dbSNP: rs61733964
NCBI 1000 Genomes Browser:
rs61733964
Molecular consequence:
  • NM_001144996.2:c.1408G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001144997.2:c.1117G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367993.1:c.1069G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367994.1:c.52G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374465.1:c.1396G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001410977.1:c.1528G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001414029.1:c.1408G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001414030.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001414031.1:c.1309G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001414032.1:c.1276G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001414033.1:c.1213G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001414034.1:c.1396G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001414035.1:c.1057G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002206.3:c.1396G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Congenital muscular dystrophy due to integrin alpha-7 deficiency
Synonyms:
MYOPATHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY; Congenital muscular dystrophy with integrin alpha-7 deficiency; Muscular dystrophy, congenital, due to ITGA7 deficiency
Identifiers:
MONDO: MONDO:0013177; MedGen: C2750786; Orphanet: 34520; OMIM: 613204

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000832716Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Aug 16, 2022) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

SCV004235822Revvity Omics, Revvity
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Jun 1, 2023) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical 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

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000832716.6

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change replaces alanine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 466 of the ITGA7 protein (p.Ala466Thr). This variant is present in population databases (rs61733964, gnomAD 0.03%). This variant has not been reported in the literature in individuals affected with ITGA7-related conditions. ClinVar contains an entry for this variant (Variation ID: 580306). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. 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.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From Revvity Omics, Revvity, SCV004235822.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024