rs7077361

chr10-15519544-T-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003638.3(ITGA8):c.2983-132A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.111 in 939,584 control chromosomes in the GnomAD database, including 6,396 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 0.10 (916 hom., cov: 32)
  • Exomes 𝑓: 0.11 (5480 hom.)
• Consequence: ITGA8 NM_003638.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.72

Genes affected

ITGA8 (HGNC:6144): (integrin subunit alpha 8) Integrins are heterodimeric transmembrane receptor proteins that mediate numerous cellular processes including cell adhesion, cytoskeletal rearrangement, and activation of cell signaling pathways. Integrins are composed of alpha and beta subunits. This gene encodes the alpha 8 subunit of the heterodimeric integrin alpha8beta1 protein. The encoded protein is a single-pass type 1 membrane protein that contains multiple FG-GAP repeats. This repeat is predicted to fold into a beta propeller structure. This gene regulates the recruitment of mesenchymal cells into epithelial structures, mediates cell-cell interactions, and regulates neurite outgrowth of sensory and motor neurons. The integrin alpha8beta1 protein thus plays an important role in wound-healing and organogenesis. Mutations in this gene have been associated with renal hypodysplasia/aplasia-1 (RHDA1) and with several animal models of chronic kidney disease. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2014]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.123 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ITGA8	NM_003638.3	c.2983-132A>G		intron_variant		ENST00000378076.4
ITGA8	NM_001291494.2	c.2938-132A>G		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ITGA8	ENST00000378076.4	c.2983-132A>G		intron_variant		1	NM_003638.3	P1

Frequencies

GnomAD3 genomes AF: 0.105 AC: 15894 AN: 152038 Hom.: 918 Cov.: 32

Gnomad AFR AF: 0.0862

Gnomad AMI AF: 0.156

Gnomad AMR AF: 0.0720

Gnomad ASJ AF: 0.134

Gnomad EAS AF: 0.00212

Gnomad SAS AF: 0.0854

Gnomad FIN AF: 0.132

Gnomad MID AF: 0.165

Gnomad NFE AF: 0.126

Gnomad OTH AF: 0.0980

GnomAD4 exome AF: 0.112 AC: 88380 AN: 787428 Hom.: 5480 AF XY: 0.112 AC XY: 46659 AN XY: 415034

Gnomad4 AFR exome AF: 0.0879

Gnomad4 AMR exome AF: 0.0543

Gnomad4 ASJ exome AF: 0.131

Gnomad4 EAS exome AF: 0.00236

Gnomad4 SAS exome AF: 0.0947

Gnomad4 FIN exome AF: 0.124

Gnomad4 NFE exome AF: 0.124

Gnomad4 OTH exome AF: 0.109

GnomAD4 genome AF: 0.104 AC: 15894 AN: 152156 Hom.: 916 Cov.: 32 AF XY: 0.104 AC XY: 7702 AN XY: 74382

Gnomad4 AFR AF: 0.0862

Gnomad4 AMR AF: 0.0720

Gnomad4 ASJ AF: 0.134

Gnomad4 EAS AF: 0.00213

Gnomad4 SAS AF: 0.0855

Gnomad4 FIN AF: 0.132

Gnomad4 NFE AF: 0.126

Gnomad4 OTH AF: 0.0974

Alfa AF: 0.122 Hom.: 2428

Bravo AF: 0.101

Asia WGS AF: 0.0370 AC: 129 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
Cadd	Benign	0.086
Dann	Benign	0.39

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: rs7077361; hg19: chr10-15561543;