ENST00000592148.1:c.329A>G

Variant names:

• chr17-76688319-T-C
• rs2286587
• ENST00000592148.1:c.329A>G

Variant summary

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

The ENST00000592148.1(MXRA7):​c.329A>G​(p.His110Arg) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.358 in 1,467,468 control chromosomes in the GnomAD database, including 96,623 homozygotes. In-silico tool predicts a benign outcome for this variant. 9/11 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.32 (8216 hom., cov: 33)
  • Exomes 𝑓: 0.36 (88407 hom.)
• Consequence: MXRA7 ENST00000592148.1 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.78
• Publications: 13 publications found

Genes affected

MXRA7 (HGNC:7541): (matrix remodeling associated 7) Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

SNHG16 (HGNC:44352): (small nucleolar RNA host gene 16)

ENSG00000296346 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (MetaRNN=3.235042E-4).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.374 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000592148.1. 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
	MXRA7	NM_198530.4	MANE Select	c.343-143A>G		intron	N/A	NP_940932.2
	MXRA7	NM_001387276.1		c.329A>G	p.His110Arg	missense	Exon 1 of 3	NP_001374205.1
	MXRA7	NM_001387277.1		c.329A>G	p.His110Arg	missense	Exon 1 of 4	NP_001374206.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MXRA7	ENST00000592148.1	TSL:1	c.329A>G	p.His110Arg	missense	Exon 1 of 3	ENSP00000465103.1
	MXRA7	ENST00000449428.7	TSL:1 MANE Select	c.343-143A>G		intron	N/A	ENSP00000391466.1
	MXRA7	ENST00000355797.7	TSL:2	c.343-143A>G		intron	N/A	ENSP00000348050.2

Frequencies

GnomAD3 genomes AF: 0.320 AC: 48699 AN: 152098 Hom.: 8189 Cov.: 33

Gnomad AFR AF: 0.234

Gnomad AMI AF: 0.295

Gnomad AMR AF: 0.339

Gnomad ASJ AF: 0.213

Gnomad EAS AF: 0.150

Gnomad SAS AF: 0.277

Gnomad FIN AF: 0.402

Gnomad MID AF: 0.215

Gnomad NFE AF: 0.378

Gnomad OTH AF: 0.317

GnomAD2 exomes AF: 0.324 AC: 29127 AN: 89902 AF XY: 0.328

Gnomad AFR exome AF: 0.237

Gnomad AMR exome AF: 0.345

Gnomad ASJ exome AF: 0.238

Gnomad EAS exome AF: 0.160

Gnomad FIN exome AF: 0.432

Gnomad NFE exome AF: 0.379

Gnomad OTH exome AF: 0.341

GnomAD4 exome AF: 0.362 AC: 476047 AN: 1315252 Hom.: 88407 Cov.: 45 AF XY: 0.359 AC XY: 230506 AN XY: 641578

African (AFR) AF: 0.231 AC: 6856 AN: 29652

American (AMR) AF: 0.343 AC: 8460 AN: 24686

Ashkenazi Jewish (ASJ) AF: 0.225 AC: 4469 AN: 19864

East Asian (EAS) AF: 0.133 AC: 4724 AN: 35534

South Asian (SAS) AF: 0.280 AC: 18810 AN: 67096

European-Finnish (FIN) AF: 0.412 AC: 13650 AN: 33156

Middle Eastern (MID) AF: 0.237 AC: 1260 AN: 5314

European-Non Finnish (NFE) AF: 0.382 AC: 399578 AN: 1045034

Other (OTH) AF: 0.332 AC: 18240 AN: 54916

GnomAD4 genome AF: 0.320 AC: 48768 AN: 152216 Hom.: 8216 Cov.: 33 AF XY: 0.320 AC XY: 23782 AN XY: 74422

African (AFR) AF: 0.235 AC: 9758 AN: 41538

American (AMR) AF: 0.339 AC: 5192 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.213 AC: 741 AN: 3472

East Asian (EAS) AF: 0.150 AC: 778 AN: 5172

South Asian (SAS) AF: 0.278 AC: 1342 AN: 4834

European-Finnish (FIN) AF: 0.402 AC: 4267 AN: 10606

Middle Eastern (MID) AF: 0.211 AC: 62 AN: 294

European-Non Finnish (NFE) AF: 0.378 AC: 25694 AN: 67980

Other (OTH) AF: 0.315 AC: 665 AN: 2114

Alfa AF: 0.350 Hom.: 38798

Bravo AF: 0.308

TwinsUK AF: 0.380 AC: 1410

ALSPAC AF: 0.381 AC: 1467

ExAC AF: 0.236 AC: 23520

Asia WGS AF: 0.223 AC: 777 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.059
BayesDel_addAF	Benign	-0.89	T
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.22
DANN	Benign	0.34
FATHMM_MKL	Benign	0.0058	N
LIST_S2	Benign	0.27	T
MetaRNN	Benign	0.00032	T
PhyloP100		-1.8
Sift4G	Benign	0.44	T
Vest4		0.067
GERP RS		-6.6
PromoterAI		0.026	Neutral
gMVP		0.0039
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: rs2286587; hg19: chr17-74684401; COSMIC: COSV63320965;