rs1861606

chr12-22296483-G-Achr12-22296483-G-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003034.4(ST8SIA1):c.237-9190C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.305 in 151,972 control chromosomes in the GnomAD database, including 7,647 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 0.31 (7647 hom., cov: 32)
• Consequence: ST8SIA1 NM_003034.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.375

Genes affected

ST8SIA1 (HGNC:10869): (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1) Gangliosides are membrane-bound glycosphingolipids containing sialic acid. Ganglioside GD3 is known to be important for cell adhesion and growth of cultured malignant cells. The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to GM3 to produce gangliosides GD3 and GT3. The encoded protein may be found in the Golgi apparatus and is a member of glycosyltransferase family 29. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2015]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.427 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ST8SIA1	NM_003034.4	c.237-9190C>T		intron_variant		ENST00000396037.9
ST8SIA1	NM_001304450.2	c.-83-9190C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ST8SIA1	ENST00000396037.9	c.237-9190C>T		intron_variant		1	NM_003034.4	P1
ST8SIA1	ENST00000261197.7	c.237-9190C>T		intron_variant, NMD_transcript_variant		1
ST8SIA1	ENST00000540824.5	c.90-9190C>T		intron_variant		4
ST8SIA1	ENST00000541868.1	c.168-9190C>T		intron_variant		3

Frequencies

GnomAD3 genomes AF: 0.305 AC: 46299 AN: 151854 Hom.: 7625 Cov.: 32

Gnomad AFR AF: 0.432

Gnomad AMI AF: 0.175

Gnomad AMR AF: 0.255

Gnomad ASJ AF: 0.288

Gnomad EAS AF: 0.338

Gnomad SAS AF: 0.393

Gnomad FIN AF: 0.193

Gnomad MID AF: 0.345

Gnomad NFE AF: 0.250

Gnomad OTH AF: 0.291

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

GnomAD4 genome AF: 0.305 AC: 46357 AN: 151972 Hom.: 7647 Cov.: 32 AF XY: 0.304 AC XY: 22617 AN XY: 74278

Gnomad4 AFR AF: 0.432

Gnomad4 AMR AF: 0.255

Gnomad4 ASJ AF: 0.288

Gnomad4 EAS AF: 0.338

Gnomad4 SAS AF: 0.392

Gnomad4 FIN AF: 0.193

Gnomad4 NFE AF: 0.250

Gnomad4 OTH AF: 0.292

Alfa AF: 0.269 Hom.: 7881

Bravo AF: 0.314

Asia WGS AF: 0.334 AC: 1160 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
Cadd	Benign	0.063
Dann	Benign	0.37

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: rs1861606; hg19: chr12-22449417;