20-10471052-G-T

Variant names:

• chr20-10471052-G-T
• rs673034
• NM_001009608.3:c.27+12821G>T

Variant summary

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

The NM_001009608.3(SLX4IP):​c.27+12821G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.372 in 152,026 control chromosomes in the GnomAD database, including 12,357 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 0.37 (12357 hom., cov: 32)
• Consequence: SLX4IP NM_001009608.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.763
• Publications: 2 publications found

Genes affected

SLX4IP (HGNC:16225): (SLX4 interacting protein)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.488 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001009608.3. 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
	SLX4IP	NM_001009608.3	MANE Select	c.27+12821G>T		intron	N/A	NP_001009608.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLX4IP	ENST00000334534.10	TSL:1 MANE Select	c.27+12821G>T		intron	N/A	ENSP00000335557.5

Frequencies

GnomAD3 genomes AF: 0.373 AC: 56625 AN: 151908 Hom.: 12359 Cov.: 32

Gnomad AFR AF: 0.177

Gnomad AMI AF: 0.581

Gnomad AMR AF: 0.382

Gnomad ASJ AF: 0.414

Gnomad EAS AF: 0.00885

Gnomad SAS AF: 0.267

Gnomad FIN AF: 0.552

Gnomad MID AF: 0.354

Gnomad NFE AF: 0.492

Gnomad OTH AF: 0.368

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

GnomAD4 genome AF: 0.372 AC: 56617 AN: 152026 Hom.: 12357 Cov.: 32 AF XY: 0.371 AC XY: 27565 AN XY: 74338

African (AFR) AF: 0.177 AC: 7337 AN: 41440

American (AMR) AF: 0.382 AC: 5836 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.414 AC: 1434 AN: 3462

East Asian (EAS) AF: 0.00887 AC: 46 AN: 5188

South Asian (SAS) AF: 0.267 AC: 1285 AN: 4816

European-Finnish (FIN) AF: 0.552 AC: 5833 AN: 10574

Middle Eastern (MID) AF: 0.342 AC: 100 AN: 292

European-Non Finnish (NFE) AF: 0.492 AC: 33449 AN: 67950

Other (OTH) AF: 0.364 AC: 767 AN: 2110

Alfa AF: 0.420 Hom.: 1909

Bravo AF: 0.352

Asia WGS AF: 0.143 AC: 496 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	0.64
DANN	Benign	0.61
PhyloP100		-0.76
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: rs673034; hg19: chr20-10451700;