rs10159620

Positions:

• chr10-115722372-G-A
• chr10-115722372-G-C
• chr10-115722372-G-T

Variant summary

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

The ENST00000355044.8(ATRNL1):​c.3796-4876G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.368 in 151,846 control chromosomes in the GnomAD database, including 11,037 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 0.37 (11037 hom., cov: 31)
• Consequence: ATRNL1 ENST00000355044.8 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.04

Genes affected

ATRNL1 (HGNC:29063): (attractin like 1) Predicted to enable carbohydrate binding activity. Predicted to be involved in several processes, including animal organ morphogenesis; cell migration; and substrate adhesion-dependent cell spreading. Predicted to act upstream of or within G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be integral component of membrane. Predicted to be active in basement membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.526 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ATRNL1	NM_207303.4	c.3796-4876G>A		intron_variant		ENST00000355044.8	NP_997186.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ATRNL1	ENST00000355044.8	c.3796-4876G>A		intron_variant		1	NM_207303.4	ENSP00000347152	P1
ATRNL1	ENST00000650603.1	c.3688-4876G>A		intron_variant, NMD_transcript_variant				ENSP00000497485

Frequencies

GnomAD3 genomes AF: 0.368 AC: 55860 AN: 151726 Hom.: 11025 Cov.: 31

Gnomad AFR AF: 0.260

Gnomad AMI AF: 0.384

Gnomad AMR AF: 0.535

Gnomad ASJ AF: 0.400

Gnomad EAS AF: 0.521

Gnomad SAS AF: 0.502

Gnomad FIN AF: 0.356

Gnomad MID AF: 0.401

Gnomad NFE AF: 0.375

Gnomad OTH AF: 0.386

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

GnomAD4 genome AF: 0.368 AC: 55899 AN: 151846 Hom.: 11037 Cov.: 31 AF XY: 0.374 AC XY: 27775 AN XY: 74218

Gnomad4 AFR AF: 0.259

Gnomad4 AMR AF: 0.536

Gnomad4 ASJ AF: 0.400

Gnomad4 EAS AF: 0.521

Gnomad4 SAS AF: 0.503

Gnomad4 FIN AF: 0.356

Gnomad4 NFE AF: 0.375

Gnomad4 OTH AF: 0.389

Alfa AF: 0.384 Hom.: 5188

Bravo AF: 0.376

Asia WGS AF: 0.498 AC: 1730 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.16
DANN	Benign	0.59

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: rs10159620; hg19: chr10-117481882;