U.S. flag

An official website of the United States government

NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu) AND not provided

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Oct 23, 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:
RCV001267916.2

Allele description [Variation Report for NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu)]

NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu)

Gene:
GRIN1:glutamate ionotropic receptor NMDA type subunit 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q34.3
Genomic location:
Preferred name:
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu)
HGVS:
  • NC_000009.12:g.137162705C>T
  • NG_011507.1:g.28549C>T
  • NM_000832.7:c.1979C>T
  • NM_001185090.2:c.2042C>T
  • NM_001185091.2:c.2042C>T
  • NM_007327.4:c.1979C>TMANE SELECT
  • NM_021569.4:c.1979C>T
  • NP_000823.4:p.Pro660Leu
  • NP_001172019.1:p.Pro681Leu
  • NP_001172020.1:p.Pro681Leu
  • NP_015566.1:p.Pro660Leu
  • NP_067544.1:p.Pro660Leu
  • NC_000009.11:g.140057157C>T
  • NC_000009.11:g.140057157C>T
  • NM_007327.3:c.1979C>T
  • p.Pro681Leu
Protein change:
P660L
Links:
dbSNP: rs1328780843
NCBI 1000 Genomes Browser:
rs1328780843
Molecular consequence:
  • NM_000832.7:c.1979C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001185090.2:c.2042C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001185091.2:c.2042C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007327.4:c.1979C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_021569.4:c.1979C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001446425Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen
criteria provided, single submitter

(ACMG Guidelines, 2015)
Likely pathogenic
(Oct 23, 2020)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot provided1not 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 Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen, SCV001446425.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyes1not providednot providednot providednot providednot providednot provided

Last Updated: Jun 23, 2024