NM_001193466.2(KANSL1):c.1857G>T (p.Arg619=) AND not specified

Clinical significance:Benign (Last evaluated: Dec 29, 2014)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000187725.1

Allele description [Variation Report for NM_001193466.2(KANSL1):c.1857G>T (p.Arg619=)]

NM_001193466.2(KANSL1):c.1857G>T (p.Arg619=)

Gene:
KANSL1:KAT8 regulatory NSL complex subunit 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
NM_001193466.2(KANSL1):c.1857G>T (p.Arg619=)
Other names:
p.R619R:CGG>CGT
HGVS:
  • NC_000017.11:g.46050696C>A
  • NG_032784.1:g.179679G>T
  • NM_001193465.1:c.1857G>T
  • NM_001193466.2:c.1857G>T
  • NM_015443.3:c.1857G>T
  • NP_001180394.1:p.Arg619=
  • NP_001180395.1:p.Arg619=
  • NP_056258.1:p.Arg619=
  • NC_000017.10:g.44128062C>A
  • NM_001193466.1:c.1857G>T
Links:
dbSNP: rs191986791
NCBI 1000 Genomes Browser:
rs191986791
Molecular consequence:
  • NM_001193465.1:c.1857G>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001193466.2:c.1857G>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_015443.3:c.1857G>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000241322GeneDxcriteria provided, single submitter
Benign
(Dec 29, 2014)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV000241322.11

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

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

Last Updated: May 23, 2021

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