8-73483804-C-T

Variant names:

• chr8-73483804-C-T
• rs4738374
• NM_001164380.2:c.1531-61102G>A

Variant summary

Our verdict is Benign. The variant received -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The NM_001164380.2(STAU2):​c.1531-61102G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.513 in 151,934 control chromosomes in the GnomAD database, including 20,307 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 0.51 (20307 hom., cov: 32)
• Consequence: STAU2 NM_001164380.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.898
• Publications: 4 publications found

Genes affected

STAU2 (HGNC:11371): (staufen double-stranded RNA binding protein 2) Staufen homolog 2 is a member of the family of double-stranded RNA (dsRNA)-binding proteins involved in the transport and/or localization of mRNAs to different subcellular compartments and/or organelles. These proteins are characterized by the presence of multiple dsRNA-binding domains which are required to bind RNAs having double-stranded secondary structures. Staufen homolog 2 shares 48.5% and 59.9% similarity with drosophila and human staufen, respectively. The exact function of Staufen homolog 2 is not known, but since it contains 3 copies of conserved dsRNA binding domain, it could be involved in double-stranded RNA binding events. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]

ACMG classification

Our verdict: Benign. The variant received -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.46).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.615 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001164380.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	STAU2	NM_001164380.2	MANE Select	c.1531-61102G>A		intron	N/A	NP_001157852.1	Q9NUL3-1
	STAU2	NM_001164381.2		c.1435-61102G>A		intron	N/A	NP_001157853.1	Q9NUL3-2
	STAU2	NM_001164382.2		c.1332+43887G>A		intron	N/A	NP_001157854.1	Q9NUL3-7

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	STAU2	ENST00000524300.6	TSL:2 MANE Select	c.1531-61102G>A		intron	N/A	ENSP00000428756.1	Q9NUL3-1
	STAU2	ENST00000522695.5	TSL:1	c.1435-61102G>A		intron	N/A	ENSP00000428456.1	Q9NUL3-2
	STAU2	ENST00000946925.1		c.1536+43887G>A		intron	N/A	ENSP00000616984.1

Frequencies

GnomAD3 genomes AF: 0.513 AC: 77900 AN: 151816 Hom.: 20275 Cov.: 32

Gnomad AFR AF: 0.465

Gnomad AMI AF: 0.349

Gnomad AMR AF: 0.625

Gnomad ASJ AF: 0.545

Gnomad EAS AF: 0.402

Gnomad SAS AF: 0.471

Gnomad FIN AF: 0.543

Gnomad MID AF: 0.383

Gnomad NFE AF: 0.526

Gnomad OTH AF: 0.506

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

GnomAD4 genome AF: 0.513 AC: 77978 AN: 151934 Hom.: 20307 Cov.: 32 AF XY: 0.516 AC XY: 38332 AN XY: 74250

African (AFR) AF: 0.465 AC: 19278 AN: 41452

American (AMR) AF: 0.626 AC: 9544 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.545 AC: 1890 AN: 3468

East Asian (EAS) AF: 0.401 AC: 2065 AN: 5150

South Asian (SAS) AF: 0.470 AC: 2267 AN: 4822

European-Finnish (FIN) AF: 0.543 AC: 5731 AN: 10562

Middle Eastern (MID) AF: 0.381 AC: 112 AN: 294

European-Non Finnish (NFE) AF: 0.526 AC: 35701 AN: 67914

Other (OTH) AF: 0.508 AC: 1072 AN: 2110

Alfa AF: 0.533 Hom.: 8394

Bravo AF: 0.521

Asia WGS AF: 0.455 AC: 1586 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.46
CADD	Benign	2.5
DANN	Benign	0.77
PhyloP100		-0.90
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: rs4738374; hg19: chr8-74396039;