rs9913017

Variant names:

• chr17-73014881-A-C
• rs9913017
• NM_139177.4:c.306+16675T>G

Your query was ambiguous. Multiple possible variants found:

• chr17-73014881-A-C
• chr17-73014881-A-T

Variant summary

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

The NM_139177.4(SLC39A11):​c.306+16675T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.703 in 152,014 control chromosomes in the GnomAD database, including 41,474 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 0.70 (41474 hom., cov: 31)
• Consequence: SLC39A11 NM_139177.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.373
• Publications: 4 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 (NFE) allele frequency at 95% confidence interval = 0.863 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SLC39A11	NM_139177.4	c.306+16675T>G		intron_variant	Intron 4 of 9	ENST00000255559.8	NP_631916.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SLC39A11	ENST00000255559.8	c.306+16675T>G		intron_variant	Intron 4 of 9	1	NM_139177.4	ENSP00000255559.3

Frequencies

GnomAD3 genomes AF: 0.703 AC: 106778 AN: 151896 Hom.: 41466 Cov.: 31

Gnomad AFR AF: 0.346

Gnomad AMI AF: 0.923

Gnomad AMR AF: 0.781

Gnomad ASJ AF: 0.853

Gnomad EAS AF: 0.802

Gnomad SAS AF: 0.859

Gnomad FIN AF: 0.717

Gnomad MID AF: 0.845

Gnomad NFE AF: 0.869

Gnomad OTH AF: 0.733

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

GnomAD4 genome AF: 0.703 AC: 106807 AN: 152014 Hom.: 41474 Cov.: 31 AF XY: 0.701 AC XY: 52056 AN XY: 74274

African (AFR) AF: 0.345 AC: 14297 AN: 41396

American (AMR) AF: 0.781 AC: 11947 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.853 AC: 2961 AN: 3472

East Asian (EAS) AF: 0.802 AC: 4137 AN: 5160

South Asian (SAS) AF: 0.859 AC: 4138 AN: 4816

European-Finnish (FIN) AF: 0.717 AC: 7575 AN: 10562

Middle Eastern (MID) AF: 0.844 AC: 248 AN: 294

European-Non Finnish (NFE) AF: 0.869 AC: 59109 AN: 67996

Other (OTH) AF: 0.734 AC: 1553 AN: 2116

Alfa AF: 0.831 Hom.: 23954

Bravo AF: 0.689

Asia WGS AF: 0.796 AC: 2765 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	3.3
DANN	Benign	0.75
PhyloP100		0.37
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: rs9913017; hg19: chr17-71011020;