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NM_002633.3(PGM1):c.1258T>C (p.Tyr420His) AND not provided

Germline classification:
Benign (2 submissions)
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:
RCV000675306.6

Allele description [Variation Report for NM_002633.3(PGM1):c.1258T>C (p.Tyr420His)]

NM_002633.3(PGM1):c.1258T>C (p.Tyr420His)

Gene:
PGM1:phosphoglucomutase 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p31.3
Genomic location:
Preferred name:
NM_002633.3(PGM1):c.1258T>C (p.Tyr420His)
HGVS:
  • NC_000001.11:g.63648630T>C
  • NG_016966.1:g.60355T>C
  • NM_001172818.1:c.1312T>C
  • NM_001172819.2:c.667T>C
  • NM_002633.3:c.1258T>CMANE SELECT
  • NP_001166289.1:p.Tyr438His
  • NP_001166290.1:p.Tyr223His
  • NP_002624.2:p.Tyr420His
  • NC_000001.10:g.64114301T>C
  • NM_002633.2:c.1258T>C
  • P36871:p.Tyr420His
Protein change:
Y223H
Links:
UniProtKB: P36871#VAR_006092; dbSNP: rs11208257
NCBI 1000 Genomes Browser:
rs11208257
Molecular consequence:
  • NM_001172818.1:c.1312T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001172819.2:c.667T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002633.3:c.1258T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000800971Mayo Clinic Laboratories, Mayo Clinic
no assertion criteria provided
Benign
(Oct 23, 2015)
unknownclinical testing

SCV005287306Breakthrough Genomics, Breakthrough Genomics
criteria provided, single submitter

(ACMG Guidelines, 2015)
Benigngermlinenot provided

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providednot provided
not providedunknownunknownnot providednot providednot providednot providednot 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 Mayo Clinic Laboratories, Mayo Clinic, SCV000800971.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

From Breakthrough Genomics, Breakthrough Genomics, SCV005287306.1

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

Last Updated: Sep 29, 2024