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NM_014159.7(SETD2):c.2603A>G (p.Asp868Gly) AND not provided

Germline classification:
Benign (2 submissions)
Last evaluated:
May 1, 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:
RCV001573515.8

Allele description [Variation Report for NM_014159.7(SETD2):c.2603A>G (p.Asp868Gly)]

NM_014159.7(SETD2):c.2603A>G (p.Asp868Gly)

Gene:
SETD2:SET domain containing 2, histone lysine methyltransferase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3p21.31
Genomic location:
Preferred name:
NM_014159.7(SETD2):c.2603A>G (p.Asp868Gly)
HGVS:
  • NC_000003.12:g.47122033T>C
  • NG_032091.1:g.46945A>G
  • NM_001349370.3:c.2471A>G
  • NM_014159.7:c.2603A>GMANE SELECT
  • NP_001336299.1:p.Asp824Gly
  • NP_054878.5:p.Asp868Gly
  • NP_054878.5:p.Asp868Gly
  • LRG_775t1:c.2603A>G
  • LRG_775:g.46945A>G
  • LRG_775p1:p.Asp868Gly
  • NC_000003.11:g.47163523T>C
  • NM_014159.6:c.2603A>G
  • NR_146158.3:n.2792A>G
Protein change:
D824G
Links:
dbSNP: rs201752182
NCBI 1000 Genomes Browser:
rs201752182
Molecular consequence:
  • NM_001349370.3:c.2471A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014159.7:c.2603A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_146158.3:n.2792A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
1

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
SCV001799508Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus
no assertion criteria provided
Likely benigngermlineclinical testing

SCV004154385CeGaT Center for Human Genetics Tuebingen
criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)
Benign
(May 1, 2022)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus, SCV001799508.1

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

From CeGaT Center for Human Genetics Tuebingen, SCV004154385.7

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

SETD2: BS1, BS2

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Jul 15, 2024