NM_152703.5(SAMD9L):c.4261C>T (p.His1421Tyr) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 30, 2023
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:: RCV002586331.3

Allele description [Variation Report for NM_152703.5(SAMD9L):c.4261C>T (p.His1421Tyr)]

NM_152703.5(SAMD9L):c.4261C>T (p.His1421Tyr)

Gene:

SAMD9L:sterile alpha motif domain containing 9 like [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q21.2

Genomic location:

Preferred name:

NM_152703.5(SAMD9L):c.4261C>T (p.His1421Tyr)

HGVS:

NC_000007.14:g.93131711G>A
NG_053186.1:g.21691C>T
NM_001303496.3:c.4261C>T
NM_001303497.3:c.4261C>T
NM_001303498.3:c.4261C>T
NM_001303500.3:c.4261C>T
NM_001350082.2:c.4261C>T
NM_001350083.2:c.4261C>T
NM_001350084.2:c.4261C>T
NM_001350085.2:c.4261C>T
NM_152703.5:c.4261C>TMANE SELECT
NP_001290425.1:p.His1421Tyr
NP_001290426.1:p.His1421Tyr
NP_001290427.1:p.His1421Tyr
NP_001290429.1:p.His1421Tyr
NP_001337011.1:p.His1421Tyr
NP_001337012.1:p.His1421Tyr
NP_001337013.1:p.His1421Tyr
NP_001337014.1:p.His1421Tyr
NP_689916.2:p.His1421Tyr
NC_000007.13:g.92761024G>A

Protein change:

H1421Y

Molecular consequence:

NM_001303496.3:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001303497.3:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001303498.3:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001303500.3:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001350082.2:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001350083.2:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001350084.2:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001350085.2:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_152703.5:c.4261C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002934882	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jun 30, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002934882

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jun 30, 2023)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV002934882.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

ClinVar contains an entry for this variant (Variation ID: 1903418). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt SAMD9L protein function. This variant has not been reported in the literature in individuals affected with SAMD9L-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.01%). This sequence change replaces histidine, which is basic and polar, with tyrosine, which is neutral and polar, at codon 1421 of the SAMD9L protein (p.His1421Tyr).

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine