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NM_015443.4(KANSL1):c.112G>A (p.Gly38Ser) AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Mar 31, 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:
RCV000863167.6

Allele description [Variation Report for NM_015443.4(KANSL1):c.112G>A (p.Gly38Ser)]

NM_015443.4(KANSL1):c.112G>A (p.Gly38Ser)

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_015443.4(KANSL1):c.112G>A (p.Gly38Ser)
HGVS:
  • NC_000017.11:g.46172032C>T
  • NG_032784.1:g.58343G>A
  • NM_001193465.2:c.112G>A
  • NM_001193466.2:c.112G>A
  • NM_001379198.1:c.112G>A
  • NM_015443.4:c.112G>AMANE SELECT
  • NP_001180394.1:p.Gly38Ser
  • NP_001180395.1:p.Gly38Ser
  • NP_001366127.1:p.Gly38Ser
  • NP_056258.1:p.Gly38Ser
  • NC_000017.10:g.44249398C>T
  • NM_001193466.1:c.112G>A
Protein change:
G38S
Links:
dbSNP: rs770738115
NCBI 1000 Genomes Browser:
rs770738115
Molecular consequence:
  • NM_001193465.2:c.112G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001193466.2:c.112G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001379198.1:c.112G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_015443.4:c.112G>A - 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
SCV000520424GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Likely benign
(Mar 31, 2020)
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, SCV000520424.5

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

Last Updated: May 7, 2024