NM_018489.3(ASH1L):c.8871C>G (p.Ile2957Met) AND Intellectual disability, autosomal dominant 52

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 14, 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:: RCV003141566.3

Allele description [Variation Report for NM_018489.3(ASH1L):c.8871C>G (p.Ile2957Met)]

NM_018489.3(ASH1L):c.8871C>G (p.Ile2957Met)

Gene:

ASH1L:ASH1 like histone lysine methyltransferase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q22

Genomic location:

Preferred name:

NM_018489.3(ASH1L):c.8871C>G (p.Ile2957Met)

HGVS:

NC_000001.11:g.155337684G>C
NM_001366177.2:c.8886C>G
NM_018489.3:c.8871C>GMANE SELECT
NP_001353106.1:p.Ile2962Met
NP_060959.2:p.Ile2957Met
NC_000001.10:g.155307475G>C

Protein change:

I2957M

Molecular consequence:

NM_001366177.2:c.8886C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_018489.3:c.8871C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Intellectual disability, autosomal dominant 52
Synonyms:: Mental retardation, autosomal dominant 52; INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 52
Identifiers:: MONDO: MONDO:0030918; MedGen: C4540478; OMIM: 617796

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003825075	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Feb 14, 2022)	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

SCV003825075

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Feb 14, 2022)

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

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 Revvity Omics, Revvity, SCV003825075.2

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

#	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: Mar 16, 2024

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