NM_019597.5(HNRNPH2):c.737A>G (p.Tyr246Cys) AND Intellectual disability, X-linked, syndromic, Bain type

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 24, 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:: RCV003131152.3

Allele description [Variation Report for NM_019597.5(HNRNPH2):c.737A>G (p.Tyr246Cys)]

NM_019597.5(HNRNPH2):c.737A>G (p.Tyr246Cys)

Genes:

RPL36A-HNRNPH2:RPL36A-HNRNPH2 readthrough [Gene - HGNC]
HNRNPH2:heterogeneous nuclear ribonucleoprotein H2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq22.1

Genomic location:

Preferred name:

NM_019597.5(HNRNPH2):c.737A>G (p.Tyr246Cys)

HGVS:

NC_000023.11:g.101412725A>G
NG_007119.1:g.239T>C
NG_016327.1:g.9523A>G
NM_001032393.3:c.737A>G
NM_001199973.2:c.*733A>G
NM_001199974.2:c.*733A>G
NM_019597.5:c.737A>GMANE SELECT
NP_001027565.1:p.Tyr246Cys
NP_062543.1:p.Tyr246Cys
LRG_672:g.239T>C
NC_000023.10:g.100667713A>G
NM_019597.4:c.737A>G

Protein change:

Y246C

Molecular consequence:

NM_001199973.2:c.*733A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001199974.2:c.*733A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001032393.3:c.737A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_019597.5:c.737A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Intellectual disability, X-linked, syndromic, Bain type (MRXSB)
Synonyms:: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE
Identifiers:: MONDO: MONDO:0010512; MedGen: C4310814; OMIM: 300986

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003808738	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Mar 24, 2020)	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

SCV003808738

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Mar 24, 2020)

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, SCV003808738.2

#	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: Sep 16, 2024

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