NM_017739.4(POMGNT1):c.1867A>G (p.Met623Val) AND Retinitis pigmentosa 76

Germline classification:: Benign (1 submission)
Last evaluated:: Oct 25, 2021
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:: RCV001789219.2

Allele description [Variation Report for NM_017739.4(POMGNT1):c.1867A>G (p.Met623Val)]

NM_017739.4(POMGNT1):c.1867A>G (p.Met623Val)

Genes:

POMGNT1:protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) [Gene - OMIM - HGNC]
TSPAN1:tetraspanin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p34.1

Genomic location:

Preferred name:

NM_017739.4(POMGNT1):c.1867A>G (p.Met623Val)

HGVS:

NC_000001.11:g.46189486T>C
NG_009205.3:g.35820A>G
NM_001243766.2:c.1867A>G
NM_001290129.2:c.1801A>G
NM_001290130.2:c.1438A>G
NM_017739.4:c.1867A>GMANE SELECT
NP_001230695.2:p.Met623Val
NP_001277058.2:p.Met601Val
NP_001277059.2:p.Met480Val
NP_060209.4:p.Met623Val
LRG_701t1:c.1867A>G
LRG_701t2:c.1867A>G
LRG_701:g.35820A>G
LRG_701p1:p.Met623Val
LRG_701p2:p.Met623Val
NC_000001.10:g.46655158T>C
NG_009205.2:g.35820=
NP_060209.3:p.Met623Val

Protein change:

M480V

Links:

dbSNP: rs6659553

NCBI 1000 Genomes Browser:

rs6659553

Molecular consequence:

NM_001243766.2:c.1867A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001290129.2:c.1801A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001290130.2:c.1438A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_017739.4:c.1867A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Retinitis pigmentosa 76 (RP76)
Identifiers:: MONDO: MONDO:0014929; MedGen: C4310704; OMIM: 617123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002031724	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Oct 25, 2021)	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

SCV002031724

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Oct 25, 2021)

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	no	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 Genome-Nilou Lab, SCV002031724.1

#	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	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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