chr17-72927624-T-C

Variant names:

• chr17-72927624-T-C
• rs2452924
• NM_139177.4:c.430+20128A>G

Variant summary

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

The ENST00000255559.8(SLC39A11):​c.430+20128A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.337 in 151,992 control chromosomes in the GnomAD database, including 9,276 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 0.34 (9276 hom., cov: 32)
• Consequence: SLC39A11 ENST00000255559.8 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.65
• Publications: 1 publications found

Genes affected

SLC39A11 (HGNC:14463): (solute carrier family 39 member 11) Predicted to enable zinc ion transmembrane transporter activity. Predicted to be involved in zinc ion transmembrane transport. Predicted to be located in Golgi apparatus; nucleus; and plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.435 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000255559.8. 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
	SLC39A11	NM_139177.4	MANE Select	c.430+20128A>G		intron	N/A	NP_631916.2
	SLC39A11	NM_001159770.2		c.451+20107A>G		intron	N/A	NP_001153242.1
	SLC39A11	NM_001352692.2		c.451+20107A>G		intron	N/A	NP_001339621.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLC39A11	ENST00000255559.8	TSL:1 MANE Select	c.430+20128A>G		intron	N/A	ENSP00000255559.3
	SLC39A11	ENST00000542342.6	TSL:2	c.451+20107A>G		intron	N/A	ENSP00000445829.2
	SLC39A11	ENST00000579732.5	TSL:2	c.430+20128A>G		intron	N/A	ENSP00000464525.1

Frequencies

GnomAD3 genomes AF: 0.337 AC: 51128 AN: 151874 Hom.: 9262 Cov.: 32

Gnomad AFR AF: 0.202

Gnomad AMI AF: 0.242

Gnomad AMR AF: 0.443

Gnomad ASJ AF: 0.320

Gnomad EAS AF: 0.397

Gnomad SAS AF: 0.332

Gnomad FIN AF: 0.408

Gnomad MID AF: 0.408

Gnomad NFE AF: 0.380

Gnomad OTH AF: 0.357

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

GnomAD4 genome AF: 0.337 AC: 51151 AN: 151992 Hom.: 9276 Cov.: 32 AF XY: 0.341 AC XY: 25290 AN XY: 74272

African (AFR) AF: 0.202 AC: 8381 AN: 41480

American (AMR) AF: 0.443 AC: 6765 AN: 15254

Ashkenazi Jewish (ASJ) AF: 0.320 AC: 1112 AN: 3470

East Asian (EAS) AF: 0.397 AC: 2052 AN: 5170

South Asian (SAS) AF: 0.331 AC: 1595 AN: 4818

European-Finnish (FIN) AF: 0.408 AC: 4300 AN: 10530

Middle Eastern (MID) AF: 0.425 AC: 124 AN: 292

European-Non Finnish (NFE) AF: 0.380 AC: 25847 AN: 67952

Other (OTH) AF: 0.357 AC: 754 AN: 2114

Alfa AF: 0.370 Hom.: 17323

Bravo AF: 0.335

Asia WGS AF: 0.361 AC: 1254 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.11
DANN	Benign	0.56
PhyloP100		-1.6
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
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: rs2452924; hg19: chr17-70923763;