rs5958338

Positions:

• chrX-123900377-A-G
• chrX-123900377-A-T

Variant summary

Our verdict is Likely benign. Variant got -6 ACMG points: 0P and 6B. BP4_Strong BP6_Moderate

The NM_001167.4(XIAP):​c.1100-116A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.58 (13383 hom., 19178 hem., cov: 23)
  • Exomes 𝑓: 0.57 (65243 hom. 91629 hem.)
  • Failed GnomAD Quality Control
• Consequence: XIAP NM_001167.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.186

Genes affected

XIAP (HGNC:592): (X-linked inhibitor of apoptosis) This gene encodes a protein that belongs to a family of apoptotic suppressor proteins. Members of this family share a conserved motif termed, baculovirus IAP repeat, which is necessary for their anti-apoptotic function. This protein functions through binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2 and inhibits apoptosis induced by menadione, a potent inducer of free radicals, and interleukin 1-beta converting enzyme. This protein also inhibits at least two members of the caspase family of cell-death proteases, caspase-3 and caspase-7. Mutations in this gene are the cause of X-linked lymphoproliferative syndrome. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 2 and 11.[provided by RefSeq, Feb 2011]

ACMG classification

Verdict is Likely_benign. Variant got -6 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BP6: Variant X-123900377-A-G is Benign according to our data. Variant chrX-123900377-A-G is described in ClinVar as [Benign]. Clinvar id is 1178358.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
XIAP	NM_001167.4	c.1100-116A>G		intron_variant		ENST00000371199.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
XIAP	ENST00000371199.8	c.1100-116A>G		intron_variant		1	NM_001167.4	P1

Frequencies

GnomAD3 genomes AF: 0.584 AC: 64594 AN: 110531 Hom.: 13383 Cov.: 23 AF XY: 0.583 AC XY: 19134 AN XY: 32799

Gnomad AFR AF: 0.637

Gnomad AMI AF: 0.432

Gnomad AMR AF: 0.582

Gnomad ASJ AF: 0.534

Gnomad EAS AF: 0.423

Gnomad SAS AF: 0.563

Gnomad FIN AF: 0.661

Gnomad MID AF: 0.608

Gnomad NFE AF: 0.563

Gnomad OTH AF: 0.581

GnomAD4 exome Data not reliable, filtered out with message: InbreedingCoeff AF: 0.571 AC: 318451 AN: 557912 Hom.: 65243 AF XY: 0.578 AC XY: 91629 AN XY: 158594

Gnomad4 AFR exome AF: 0.641

Gnomad4 AMR exome AF: 0.561

Gnomad4 ASJ exome AF: 0.538

Gnomad4 EAS exome AF: 0.367

Gnomad4 SAS exome AF: 0.596

Gnomad4 FIN exome AF: 0.652

Gnomad4 NFE exome AF: 0.573

Gnomad4 OTH exome AF: 0.577

GnomAD4 genome Data not reliable, filtered out with message: InbreedingCoeff AF: 0.585 AC: 64636 AN: 110580 Hom.: 13383 Cov.: 23 AF XY: 0.584 AC XY: 19178 AN XY: 32858

Gnomad4 AFR AF: 0.637

Gnomad4 AMR AF: 0.582

Gnomad4 ASJ AF: 0.534

Gnomad4 EAS AF: 0.423

Gnomad4 SAS AF: 0.566

Gnomad4 FIN AF: 0.661

Gnomad4 NFE AF: 0.563

Gnomad4 OTH AF: 0.583

Alfa AF: 0.573 Hom.: 4407

Bravo AF: 0.584

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 19, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.26
DANN	Benign	0.67

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

Publications

LitVar

Other links and lift over

dbSNP: rs5958338; hg19: chrX-123034227; COSMIC: COSV63024519;