chr5-157460125-A-G

Position:

• chr5-157460125-A-G

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The ENST00000517951.5(ADAM19):​c.*1741+28140T>C variant causes a intron, NMD transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.351 in 1,410,364 control chromosomes in the GnomAD database, including 90,158 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.38 (11148 hom., cov: 33)
  • Exomes 𝑓: 0.35 (79010 hom.)
• Consequence: ADAM19 ENST00000517951.5 intron, NMD_transcript
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:5
• Conservation: PhyloP100: 0.658

Genes affected

ADAM19 (HGNC:197): (ADAM metallopeptidase domain 19) This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This member is a type I transmembrane protein and serves as a marker for dendritic cell differentiation. It has been demonstrated to be an active metalloproteinase, which may be involved in normal physiological processes such as cell migration, cell adhesion, cell-cell and cell-matrix interactions, and signal transduction. It is proposed to play a role in pathological processes, such as cancer, inflammatory diseases, renal diseases, and Alzheimer's disease. [provided by RefSeq, May 2013]

NIPAL4-DT (HGNC:):

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.73).
• BP6: Variant 5-157460125-A-G is Benign according to our data. Variant chr5-157460125-A-G is described in ClinVar as [Benign]. Clinvar id is 257433.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-157460125-A-G is described in Lovd as [Benign].
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.701 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
NIPAL4-DT	NR_136205.1			upstream_gene_variant
NIPAL4-DT	NR_136204.1			upstream_gene_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ADAM19	ENST00000517951.5	c.*1741+28140T>C		intron_variant, NMD_transcript_variant		2		ENSP00000428376

Frequencies

GnomAD3 genomes AF: 0.376 AC: 57139 AN: 151908 Hom.: 11131 Cov.: 33

Gnomad AFR AF: 0.392

Gnomad AMI AF: 0.422

Gnomad AMR AF: 0.360

Gnomad ASJ AF: 0.368

Gnomad EAS AF: 0.720

Gnomad SAS AF: 0.363

Gnomad FIN AF: 0.346

Gnomad MID AF: 0.361

Gnomad NFE AF: 0.350

Gnomad OTH AF: 0.373

GnomAD3 exomes AF: 0.368 AC: 17039 AN: 46260 Hom.: 3459 AF XY: 0.371 AC XY: 8811 AN XY: 23770

Gnomad AFR exome AF: 0.373

Gnomad AMR exome AF: 0.304

Gnomad ASJ exome AF: 0.328

Gnomad EAS exome AF: 0.711

Gnomad SAS exome AF: 0.357

Gnomad FIN exome AF: 0.347

Gnomad NFE exome AF: 0.333

Gnomad OTH exome AF: 0.371

GnomAD4 exome AF: 0.348 AC: 438407 AN: 1258338 Hom.: 79010 Cov.: 28 AF XY: 0.348 AC XY: 212080 AN XY: 609606

Gnomad4 AFR exome AF: 0.385

Gnomad4 AMR exome AF: 0.317

Gnomad4 ASJ exome AF: 0.362

Gnomad4 EAS exome AF: 0.671

Gnomad4 SAS exome AF: 0.348

Gnomad4 FIN exome AF: 0.345

Gnomad4 NFE exome AF: 0.338

Gnomad4 OTH exome AF: 0.361

GnomAD4 genome AF: 0.376 AC: 57188 AN: 152026 Hom.: 11148 Cov.: 33 AF XY: 0.379 AC XY: 28202 AN XY: 74318

Gnomad4 AFR AF: 0.392

Gnomad4 AMR AF: 0.360

Gnomad4 ASJ AF: 0.368

Gnomad4 EAS AF: 0.720

Gnomad4 SAS AF: 0.362

Gnomad4 FIN AF: 0.346

Gnomad4 NFE AF: 0.350

Gnomad4 OTH AF: 0.374

Alfa AF: 0.363 Hom.: 1591

Bravo AF: 0.373

Asia WGS AF: 0.537 AC: 1868 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:5

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not specified Benign:3

Benign, no assertion criteria provided	clinical testing	Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	-	- -
Benign, criteria provided, single submitter	clinical testing	PreventionGenetics, part of Exact Sciences	-	- -
Benign, no assertion criteria provided	clinical testing	Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	-	- -

Autosomal recessive congenital ichthyosis 6 Benign:1

Benign, criteria provided, single submitter

clinical testing

Illumina Laboratory Services, Illumina

Jan 13, 2018

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease. -

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Mar 03, 2015

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.73
CADD	Benign	11
DANN	Benign	0.72

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

Publications

LitVar

Other links and lift over

dbSNP: rs1105282; hg19: chr5-156887133;