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NM_015338.6(ASXL1):c.3235T>C (p.Ser1079Pro) AND Inborn genetic diseases

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jan 4, 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:
RCV002538621.2

Allele description [Variation Report for NM_015338.6(ASXL1):c.3235T>C (p.Ser1079Pro)]

NM_015338.6(ASXL1):c.3235T>C (p.Ser1079Pro)

Gene:
ASXL1:ASXL transcriptional regulator 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
20q11.21
Genomic location:
Preferred name:
NM_015338.6(ASXL1):c.3235T>C (p.Ser1079Pro)
HGVS:
  • NC_000020.11:g.32435947T>C
  • NG_027868.1:g.82604T>C
  • NM_001363734.1:c.3052T>C
  • NM_015338.6:c.3235T>CMANE SELECT
  • NP_001350663.1:p.Ser1018Pro
  • NP_056153.2:p.Ser1079Pro
  • LRG_630t1:c.3235T>C
  • LRG_630:g.82604T>C
  • NC_000020.10:g.31023750T>C
  • NM_015338.5:c.3235T>C
Protein change:
S1018P
Links:
dbSNP: rs778886643
NCBI 1000 Genomes Browser:
rs778886643
Molecular consequence:
  • NM_001363734.1:c.3052T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_015338.6:c.3235T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003684508Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Jan 4, 2022) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003684508.2

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: Sep 29, 2024