rs7092269

Variant names:

• chr10-70723063-C-T
• rs7092269
• NM_080722.4:c.871-6231C>T

Variant summary

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

The NM_080722.4(ADAMTS14):​c.871-6231C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0441 in 152,300 control chromosomes in the GnomAD database, including 185 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 0.044 (185 hom., cov: 33)
• Consequence: ADAMTS14 NM_080722.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.555
• Publications: 2 publications found

Genes affected

ADAMTS14 (HGNC:14899): (ADAM metallopeptidase with thrombospondin type 1 motif 14) This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme cleaves amino-terminal propeptides from type I procollagen, a necessary step in the formation of collagen fibers. Mutations in this gene may be associated with osteoarthritis in human patients. [provided by RefSeq, May 2016]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.0697 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_080722.4. 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
	ADAMTS14	NM_080722.4	MANE Select	c.871-6231C>T		intron	N/A	NP_542453.2	Q8WXS8-1
	ADAMTS14	NM_139155.3		c.871-6231C>T		intron	N/A	NP_631894.2	Q8WXS8-4

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ADAMTS14	ENST00000373207.2	TSL:1 MANE Select	c.871-6231C>T		intron	N/A	ENSP00000362303.1	Q8WXS8-1
	ADAMTS14	ENST00000886732.1		c.871-6231C>T		intron	N/A	ENSP00000556791.1
	ADAMTS14	ENST00000373208.5	TSL:2	c.871-6231C>T		intron	N/A	ENSP00000362304.1	Q8WXS8-4

Frequencies

GnomAD3 genomes AF: 0.0442 AC: 6730 AN: 152182 Hom.: 185 Cov.: 33

Gnomad AFR AF: 0.0232

Gnomad AMI AF: 0.0230

Gnomad AMR AF: 0.0356

Gnomad ASJ AF: 0.0343

Gnomad EAS AF: 0.000577

Gnomad SAS AF: 0.0771

Gnomad FIN AF: 0.0737

Gnomad MID AF: 0.0601

Gnomad NFE AF: 0.0561

Gnomad OTH AF: 0.0454

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

GnomAD4 genome AF: 0.0441 AC: 6724 AN: 152300 Hom.: 185 Cov.: 33 AF XY: 0.0458 AC XY: 3415 AN XY: 74484

African (AFR) AF: 0.0231 AC: 962 AN: 41560

American (AMR) AF: 0.0356 AC: 544 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.0343 AC: 119 AN: 3472

East Asian (EAS) AF: 0.000578 AC: 3 AN: 5188

South Asian (SAS) AF: 0.0761 AC: 367 AN: 4824

European-Finnish (FIN) AF: 0.0737 AC: 783 AN: 10618

Middle Eastern (MID) AF: 0.0612 AC: 18 AN: 294

European-Non Finnish (NFE) AF: 0.0561 AC: 3813 AN: 68018

Other (OTH) AF: 0.0444 AC: 94 AN: 2116

Alfa AF: 0.0535 Hom.: 401

Bravo AF: 0.0404

Asia WGS AF: 0.0410 AC: 144 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	3.8
DANN	Benign	0.42
PhyloP100		0.56
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: rs7092269; hg19: chr10-72482819;