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NM_133642.5(LARGE1):c.1788G>A (p.Ala596=) AND not specified

Germline classification:
Benign/Likely benign (2 submissions)
Last evaluated:
Oct 22, 2015
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:
RCV000153443.20

Allele description [Variation Report for NM_133642.5(LARGE1):c.1788G>A (p.Ala596=)]

NM_133642.5(LARGE1):c.1788G>A (p.Ala596=)

Gene:
LARGE1:LARGE xylosyl- and glucuronyltransferase 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q12.3
Genomic location:
Preferred name:
NM_133642.5(LARGE1):c.1788G>A (p.Ala596=)
HGVS:
  • NC_000022.11:g.33283291C>T
  • NG_009929.2:g.642138G>A
  • NM_001362949.2:c.1788G>A
  • NM_001362951.2:c.1788G>A
  • NM_001362953.2:c.1788G>A
  • NM_001378624.1:c.1788G>A
  • NM_001378625.1:c.1788G>A
  • NM_001378626.1:c.1788G>A
  • NM_001378627.1:c.1731-6036G>A
  • NM_001378628.1:c.1731-6036G>A
  • NM_001378629.1:c.1632G>A
  • NM_001378630.1:c.1185G>A
  • NM_001378631.1:c.972-6036G>A
  • NM_004737.5:c.1788G>A
  • NM_004737.7:c.1788G>A
  • NM_133642.5:c.1788G>AMANE SELECT
  • NP_001349878.1:p.Ala596=
  • NP_001349880.1:p.Ala596=
  • NP_001349882.1:p.Ala596=
  • NP_001365553.1:p.Ala596=
  • NP_001365554.1:p.Ala596=
  • NP_001365555.1:p.Ala596=
  • NP_001365558.1:p.Ala544=
  • NP_001365559.1:p.Ala395=
  • NP_004728.1:p.Ala596=
  • NP_598397.1:p.Ala596=
  • LRG_856t1:c.1788G>A
  • LRG_856t2:c.1788G>A
  • LRG_856:g.642138G>A
  • LRG_856p1:p.Ala596=
  • LRG_856p2:p.Ala596=
  • NC_000022.10:g.33679277C>T
  • NM_004737.4:c.1788G>A
  • NP_004728.1:p.(=)
  • p.Ala596Ala
Links:
dbSNP: rs74550830
NCBI 1000 Genomes Browser:
rs74550830
Molecular consequence:
  • NM_001378627.1:c.1731-6036G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001378628.1:c.1731-6036G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001378631.1:c.972-6036G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001362949.2:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001362951.2:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001362953.2:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001378624.1:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001378625.1:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001378626.1:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001378629.1:c.1632G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001378630.1:c.1185G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_004737.7:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_133642.5:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
2

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000202944Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL Classification Definitions 2015)
Benign
(Jan 24, 2014)
germlineclinical testing

Citation Link,

SCV000595558Genetic Services Laboratory, University of Chicago
criteria provided, single submitter

(ACMG Guidelines, 2015)
Likely benign
(Oct 22, 2015)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenonot providednot providednot providednot providednot providedclinical testing
not providedgermlineunknown2not providednot providednot providednot providedclinical testing

Citations

PubMed

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 Eurofins Ntd Llc (ga), SCV000202944.7

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided2not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided2not providednot providednot provided

From Genetic Services Laboratory, University of Chicago, SCV000595558.1

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

Last Updated: Jul 15, 2024