chr5-177283863-C-T

Variant names:

• chr5-177283863-C-T
• rs587784181
• NM_022455.5:c.6086C>T

Variant summary

Our verdict is Likely pathogenic. The variant received 7 ACMG points: 7P and 0B. PM1 PM2 PP3_Moderate PP5

The NM_022455.5(NSD1):​c.6086C>T​(p.Thr2029Ile) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Conflicting classifications of pathogenicity (no stars). Synonymous variant affecting the same amino acid position (i.e. T2029T) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: NSD1 NM_022455.5 missense
• Clinical Significance: Conflicting classifications of pathogenicity criteria provided, conflicting classifications P:2 U:1
• Conservation: PhyloP100: 7.86
• Publications: 1 publications found

Genes affected

NSD1 (HGNC:14234): (nuclear receptor binding SET domain protein 1) This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Sep 2018]

NSD1 Gene-Disease associations (from GenCC):

• Beckwith-Wiedemann syndrome due to NSD1 mutation

  Inheritance: AD Classification: DEFINITIVE Submitted by: G2P
• Sotos syndrome

  Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: Orphanet, G2P, ClinGen
• Sotos syndrome 1

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Labcorp Genetics (formerly Invitae), Genomics England PanelApp, Ambry Genetics

ACMG classification

Our verdict: Likely_pathogenic. The variant received 7 ACMG points.

• PM1: In a strand (size 8) in uniprot entity NSD1_HUMAN there are 4 pathogenic changes around while only 0 benign (100%) in NM_022455.5
• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.888
• PP5: Variant 5-177283863-C-T is Pathogenic according to our data. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402. Variant chr5-177283863-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 159402.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NSD1	NM_022455.5	c.6086C>T	p.Thr2029Ile	missense_variant	Exon 20 of 23	ENST00000439151.7	NP_071900.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NSD1	ENST00000439151.7	c.6086C>T	p.Thr2029Ile	missense_variant	Exon 20 of 23	1	NM_022455.5	ENSP00000395929.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

Alfa AF: 0.00 Hom.: 0

ClinVar

Significance: Conflicting classifications of pathogenicity

Submissions summary: Pathogenic:2 Uncertain:1

Revision: criteria provided, conflicting classifications

Submissions by phenotype

not provided Pathogenic:1 Uncertain:1

May 31, 2023

GeneDx

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge -

Apr 18, 2019

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Likely pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has been observed to be de novo in an individual with clinical features of Sotos syndrome (Invitae). ClinVar contains an entry for this variant (Variation ID: 159402). This variant is not present in population databases (ExAC no frequency). This sequence change replaces threonine with isoleucine at codon 2029 of the NSD1 protein (p.Thr2029Ile). The threonine residue is highly conserved and there is a moderate physicochemical difference between threonine and isoleucine. -

Sotos syndrome Pathogenic:1

Feb 08, 2013

Genetic Services Laboratory, University of Chicago

Significance: Likely pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	1.0
BayesDel_addAF	Pathogenic	0.39	D
BayesDel_noAF	Pathogenic	0.32
CADD	Pathogenic	31
DANN	Pathogenic	1.0
DEOGEN2	Uncertain	0.67	.;D;.
Eigen	Pathogenic	0.81
Eigen_PC	Pathogenic	0.80
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Pathogenic	0.98	D;D;.
M_CAP	Uncertain	0.16	D
MetaRNN	Pathogenic	0.89	D;D;D
MetaSVM	Uncertain	0.35	D
MutationAssessor	Benign	1.7	.;L;.
PhyloP100		7.9
PrimateAI	Pathogenic	0.93	D
PROVEAN	Pathogenic	-5.4	D;D;D
REVEL	Pathogenic	0.81
Sift	Uncertain	0.0050	D;D;D
Sift4G	Pathogenic	0.0010	D;D;D
Polyphen		1.0	D;D;D
Vest4		0.88
MutPred		0.67		.;Loss of ubiquitination at K2031 (P = 0.0506);.;
MVP		0.90
MPC		2.7
ClinPred		1.0	D
GERP RS		5.4
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Varity_R		0.86
gMVP		0.92
Mutation Taster		=27/73	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs587784181; hg19: chr5-176710864;