chr15-92409060-G-A

Variant names:

• chr15-92409060-G-A
• rs4777974
• NM_006011.4:c.98+14898G>A

Variant summary

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

The NM_006011.4(ST8SIA2):​c.98+14898G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.646 in 152,038 control chromosomes in the GnomAD database, including 32,231 homozygotes. 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 0.65 (32231 hom., cov: 32)
• Consequence: ST8SIA2 NM_006011.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.201
• Publications: 6 publications found

Genes affected

ST8SIA2 (HGNC:10870): (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2) The protein encoded by this gene is a type II membrane protein that is thought to catalyze the transfer of sialic acid from CMP-sialic acid to N-linked oligosaccharides and glycoproteins. The encoded protein may be found in the Golgi apparatus and may be involved in the production of polysialic acid, a modulator of the adhesive properties of neural cell adhesion molecule (NCAM1). This protein is a member of glycosyltransferase family 29. [provided by RefSeq, Jul 2008]

ST8SIA2 Gene-Disease associations (from GenCC):

• schizophrenia

  Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.838 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006011.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ST8SIA2	NM_006011.4	MANE Select	c.98+14898G>A		intron	N/A	NP_006002.1
	ST8SIA2	NM_001330416.2		c.98+14898G>A		intron	N/A	NP_001317345.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ST8SIA2	ENST00000268164.8	TSL:1 MANE Select	c.98+14898G>A		intron	N/A	ENSP00000268164.3
	ST8SIA2	ENST00000539113.5	TSL:1	c.98+14898G>A		intron	N/A	ENSP00000437382.1
	ST8SIA2	ENST00000957924.1		c.218+6089G>A		intron	N/A	ENSP00000627983.1

Frequencies

GnomAD3 genomes AF: 0.646 AC: 98136 AN: 151920 Hom.: 32205 Cov.: 32

Gnomad AFR AF: 0.682

Gnomad AMI AF: 0.492

Gnomad AMR AF: 0.744

Gnomad ASJ AF: 0.591

Gnomad EAS AF: 0.859

Gnomad SAS AF: 0.677

Gnomad FIN AF: 0.554

Gnomad MID AF: 0.665

Gnomad NFE AF: 0.602

Gnomad OTH AF: 0.659

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

GnomAD4 genome AF: 0.646 AC: 98219 AN: 152038 Hom.: 32231 Cov.: 32 AF XY: 0.651 AC XY: 48375 AN XY: 74314

African (AFR) AF: 0.682 AC: 28282 AN: 41462

American (AMR) AF: 0.744 AC: 11370 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.591 AC: 2052 AN: 3470

East Asian (EAS) AF: 0.859 AC: 4440 AN: 5168

South Asian (SAS) AF: 0.676 AC: 3259 AN: 4818

European-Finnish (FIN) AF: 0.554 AC: 5857 AN: 10564

Middle Eastern (MID) AF: 0.660 AC: 194 AN: 294

European-Non Finnish (NFE) AF: 0.602 AC: 40931 AN: 67972

Other (OTH) AF: 0.659 AC: 1385 AN: 2102

Alfa AF: 0.624 Hom.: 6810

Bravo AF: 0.661

Asia WGS AF: 0.765 AC: 2656 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.54
DANN	Benign	0.74
PhyloP100		-0.20
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: rs4777974; hg19: chr15-92952290;