NM_006279.5:c.782G>T

Variant names:

• chr1-43920441-G-T
• NM_006279.5:c.782G>T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_006279.5(ST3GAL3):​c.782G>T​(p.Arg261Leu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. R261Q) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: ST3GAL3 NM_006279.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.83

Genes affected

ST3GAL3 (HGNC:10866): (ST3 beta-galactoside alpha-2,3-sialyltransferase 3) The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with a form of autosomal recessive nonsymdromic cognitive disability as well as infantile epileptic encephalopathy. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]

ENSG00000284989 (HGNC:):

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.15880838).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ST3GAL3	NM_006279.5	c.782G>T	p.Arg261Leu	missense_variant	Exon 10 of 12	ENST00000347631.8	NP_006270.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ST3GAL3	ENST00000347631.8	c.782G>T	p.Arg261Leu	missense_variant	Exon 10 of 12	5	NM_006279.5	ENSP00000317192.6
ENSG00000284989	ENST00000645057.1	n.*2104G>T		non_coding_transcript_exon_variant	Exon 24 of 26			ENSP00000494063.1
ENSG00000284989	ENST00000645057.1	n.*2104G>T		3_prime_UTR_variant	Exon 24 of 26			ENSP00000494063.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.17
BayesDel_addAF	Benign	-0.10	T
BayesDel_noAF	Benign	-0.38
CADD	Uncertain	25
DANN	Uncertain	1.0
DEOGEN2	Benign	0.12	T;.;.;.;.;.;.;.;T;.;.;.;.;T;.;.;.
Eigen	Benign	-0.25
Eigen_PC	Benign	-0.077
FATHMM_MKL	Benign	0.73	D
LIST_S2	Uncertain	0.89	.;D;D;D;D;D;D;D;.;D;D;D;D;D;D;D;D
MetaRNN	Benign	0.16	T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T
MetaSVM	Benign	-1.1	T
MutationAssessor	Benign	0.30	N;.;.;.;.;.;.;.;N;.;.;.;.;N;.;.;.
PrimateAI	Uncertain	0.55	T
PROVEAN	Benign	-1.4	.;N;N;N;.;.;.;.;.;.;N;.;.;.;N;.;.
REVEL	Benign	0.10
Sift	Benign	0.096	.;T;T;T;.;.;.;.;.;.;T;.;.;.;T;.;.
Sift4G	Benign	0.68	.;T;T;T;.;.;.;.;.;.;T;.;.;.;T;.;.
Polyphen		0.0030	B;B;B;B;.;.;B;B;B;.;B;.;.;B;.;.;.
Vest4		0.28, 0.28, 0.30, 0.31, 0.27
MutPred		0.58		Loss of methylation at R261 (P = 0.0304);.;.;.;Loss of methylation at R261 (P = 0.0304);.;.;.;Loss of methylation at R261 (P = 0.0304);Loss of methylation at R261 (P = 0.0304);.;.;Loss of methylation at R261 (P = 0.0304);Loss of methylation at R261 (P = 0.0304);.;.;.;
MVP		0.28
MPC		0.73
ClinPred		0.44	T
GERP RS		4.6
Varity_R		0.13
gMVP		0.74

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.020		Details are displayed if max score is > 0.2

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr1-44386113;