NM_001320752.2:c.-4-13123A>G

Variant names:

• chrX-7240073-A-G
• rs2017591
• NM_001320752.2:c.-4-13123A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001320752.2(STS):​c.-4-13123A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.36 (5256 hom., 10540 hem., cov: 20)
• Consequence: STS NM_001320752.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.347
• Publications: 4 publications found

Genes affected

STS (HGNC:11425): (steroid sulfatase) This gene encodes a multi-pass membrane protein that is localized to the endoplasmic reticulum. It belongs to the sulfatase family and hydrolyzes several 3-beta-hydroxysteroid sulfates, which serve as metabolic precursors for estrogens, androgens, and cholesterol. Mutations in this gene are associated with X-linked ichthyosis (XLI). Alternatively spliced transcript variants resulting from the use of different promoters have been described for this gene (PMID:17601726). [provided by RefSeq, Mar 2016]

STS Gene-Disease associations (from GenCC):

• recessive X-linked ichthyosis

  Inheritance: XL Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: G2P, Orphanet, Genomics England PanelApp, Labcorp Genetics (formerly Invitae)

ENSG00000293893 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.39 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
STS	NM_001320752.2	c.-4-13123A>G		intron_variant	Intron 2 of 10	ENST00000674429.1	NP_001307681.2
STS	NM_001320750.3	c.33-13123A>G		intron_variant	Intron 2 of 10		NP_001307679.1
STS	NM_001320751.2	c.33-13123A>G		intron_variant	Intron 3 of 11		NP_001307680.1
STS	NM_000351.7	c.-4-13123A>G		intron_variant	Intron 1 of 9		NP_000342.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
STS	ENST00000674429.1	c.-4-13123A>G		intron_variant	Intron 2 of 10		NM_001320752.2	ENSP00000501534.1

Frequencies

GnomAD3 genomes AF: 0.360 AC: 38780 AN: 107755 Hom.: 5256 Cov.: 20

Gnomad AFR AF: 0.303

Gnomad AMI AF: 0.638

Gnomad AMR AF: 0.338

Gnomad ASJ AF: 0.351

Gnomad EAS AF: 0.396

Gnomad SAS AF: 0.224

Gnomad FIN AF: 0.382

Gnomad MID AF: 0.376

Gnomad NFE AF: 0.394

Gnomad OTH AF: 0.371

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.360 AC: 38775 AN: 107805 Hom.: 5256 Cov.: 20 AF XY: 0.348 AC XY: 10540 AN XY: 30295

African (AFR) AF: 0.303 AC: 8935 AN: 29525

American (AMR) AF: 0.338 AC: 3377 AN: 9988

Ashkenazi Jewish (ASJ) AF: 0.351 AC: 916 AN: 2609

East Asian (EAS) AF: 0.397 AC: 1332 AN: 3353

South Asian (SAS) AF: 0.224 AC: 539 AN: 2411

European-Finnish (FIN) AF: 0.382 AC: 2065 AN: 5412

Middle Eastern (MID) AF: 0.361 AC: 78 AN: 216

European-Non Finnish (NFE) AF: 0.394 AC: 20562 AN: 52163

Other (OTH) AF: 0.374 AC: 548 AN: 1465

Alfa AF: 0.339 Hom.: 2149

Bravo AF: 0.362

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	3.2
DANN	Benign	0.46
PhyloP100		0.35
Mutation Taster		=100/0	polymorphism (auto)

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: rs2017591; hg19: chrX-7158114;