NM_017730.4(QRICH1):c.1498A>G (p.Arg500Gly) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 26, 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:: RCV002221942.3

Allele description [Variation Report for NM_017730.4(QRICH1):c.1498A>G (p.Arg500Gly)]

NM_017730.4(QRICH1):c.1498A>G (p.Arg500Gly)

Gene:

QRICH1:glutamine rich 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Preferred name:

NM_017730.4(QRICH1):c.1498A>G (p.Arg500Gly)

HGVS:

NC_000003.12:g.49047087T>C
NM_001320580.2:c.1498A>G
NM_001320581.2:c.1498A>G
NM_001320582.2:c.1498A>G
NM_001320583.2:c.1498A>G
NM_001320584.1:c.1498A>G
NM_001320585.1:c.1498A>G
NM_017730.4:c.1498A>G
NM_198880.3:c.1498A>GMANE SELECT
NP_001307509.1:p.Arg500Gly
NP_001307510.1:p.Arg500Gly
NP_001307511.1:p.Arg500Gly
NP_001307512.1:p.Arg500Gly
NP_001307513.1:p.Arg500Gly
NP_001307514.1:p.Arg500Gly
NP_060200.2:p.Arg500Gly
NP_942581.1:p.Arg500Gly
NC_000003.11:g.49084520T>C
NM_017730.3:c.1498A>G

Protein change:

R500G

Links:

dbSNP: rs2093343142

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002499227	Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jan 26, 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

SCV002499227

Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jan 26, 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	yes	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 Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center, SCV002499227.1

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

Description

PP2, PP3, PM2

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 24, 2023

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