5-179177376-C-T

Variant names:

• chr5-179177376-C-T
• rs4701077
• NM_014244.5:c.975+3696G>A

Variant summary

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

The NM_014244.5(ADAMTS2):​c.975+3696G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.381 in 152,076 control chromosomes in the GnomAD database, including 11,931 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 0.38 (11931 hom., cov: 33)
• Consequence: ADAMTS2 NM_014244.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.346
• Publications: 4 publications found

Genes affected

ADAMTS2 (HGNC:218): (ADAM metallopeptidase with thrombospondin type 1 motif 2) This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) 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 procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]

ADAMTS2 Gene-Disease associations (from GenCC):

• Ehlers-Danlos syndrome, dermatosparaxis type

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), Genomics England PanelApp, Orphanet, G2P, PanelApp Australia, Illumina

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 (EAS) allele frequency at 95% confidence interval = 0.745 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ADAMTS2	NM_014244.5	c.975+3696G>A		intron_variant	Intron 5 of 21	ENST00000251582.12	NP_055059.2
ADAMTS2	NM_021599.4	c.975+3696G>A		intron_variant	Intron 5 of 10		NP_067610.1
ADAMTS2	XM_047417895.1	c.480+3696G>A		intron_variant	Intron 4 of 20		XP_047273851.1
ADAMTS2	XM_047417896.1	c.93+3696G>A		intron_variant	Intron 3 of 19		XP_047273852.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ADAMTS2	ENST00000251582.12	c.975+3696G>A		intron_variant	Intron 5 of 21	1	NM_014244.5	ENSP00000251582.7
ADAMTS2	ENST00000274609.5	c.975+3696G>A		intron_variant	Intron 5 of 10	1		ENSP00000274609.5
ADAMTS2	ENST00000518335.3	c.975+3696G>A		intron_variant	Intron 5 of 20	3		ENSP00000489888.2
ADAMTS2	ENST00000698889.1	n.975+3696G>A		intron_variant	Intron 5 of 20			ENSP00000514008.1

Frequencies

GnomAD3 genomes AF: 0.381 AC: 57957 AN: 151958 Hom.: 11917 Cov.: 33

Gnomad AFR AF: 0.281

Gnomad AMI AF: 0.410

Gnomad AMR AF: 0.515

Gnomad ASJ AF: 0.331

Gnomad EAS AF: 0.765

Gnomad SAS AF: 0.522

Gnomad FIN AF: 0.319

Gnomad MID AF: 0.487

Gnomad NFE AF: 0.383

Gnomad OTH AF: 0.424

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

GnomAD4 genome AF: 0.381 AC: 57998 AN: 152076 Hom.: 11931 Cov.: 33 AF XY: 0.383 AC XY: 28467 AN XY: 74352

African (AFR) AF: 0.281 AC: 11664 AN: 41480

American (AMR) AF: 0.516 AC: 7886 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.331 AC: 1148 AN: 3468

East Asian (EAS) AF: 0.765 AC: 3954 AN: 5168

South Asian (SAS) AF: 0.524 AC: 2521 AN: 4814

European-Finnish (FIN) AF: 0.319 AC: 3368 AN: 10574

Middle Eastern (MID) AF: 0.480 AC: 141 AN: 294

European-Non Finnish (NFE) AF: 0.383 AC: 26037 AN: 67972

Other (OTH) AF: 0.429 AC: 905 AN: 2112

Alfa AF: 0.388 Hom.: 39884

Bravo AF: 0.394

Asia WGS AF: 0.597 AC: 2078 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	2.5
DANN	Benign	0.74
PhyloP100		-0.35
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: rs4701077; hg19: chr5-178604377;