rs10790218

chr11-117871280-G-A

Variant summary

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

The NM_022003.4(FXYD6):c.-6+5312C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.433 in 152,010 control chromosomes in the GnomAD database, including 14,558 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 0.43 (14558 hom., cov: 32)
• Consequence: FXYD6 NM_022003.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.268

Genes affected

FXYD6 (HGNC:4030): (FXYD domain containing ion transport regulator 6) This gene encodes a member of the FXYD family of transmembrane proteins. This particular protein encodes phosphohippolin, which likely affects the activity of Na,K-ATPase. Multiple alternatively spliced transcript variants encoding the same protein have been described. Related pseudogenes have been identified on chromosomes 10 and X. Read-through transcripts have been observed between this locus and the downstream sodium/potassium-transporting ATPase subunit gamma (FXYD2, GeneID 486) locus.[provided by RefSeq, Feb 2011]

FXYD6-FXYD2 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.521 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FXYD6	NM_022003.4	c.-6+5312C>T		intron_variant		ENST00000526014.6
FXYD6-FXYD2	NM_001243598.4	c.-6+5312C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FXYD6	ENST00000526014.6	c.-6+5312C>T		intron_variant		1	NM_022003.4	P1

Frequencies

GnomAD3 genomes AF: 0.433 AC: 65715 AN: 151892 Hom.: 14544 Cov.: 32

Gnomad AFR AF: 0.490

Gnomad AMI AF: 0.574

Gnomad AMR AF: 0.492

Gnomad ASJ AF: 0.429

Gnomad EAS AF: 0.538

Gnomad SAS AF: 0.412

Gnomad FIN AF: 0.436

Gnomad MID AF: 0.389

Gnomad NFE AF: 0.376

Gnomad OTH AF: 0.426

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

GnomAD4 genome AF: 0.433 AC: 65768 AN: 152010 Hom.: 14558 Cov.: 32 AF XY: 0.437 AC XY: 32443 AN XY: 74284

Gnomad4 AFR AF: 0.490

Gnomad4 AMR AF: 0.493

Gnomad4 ASJ AF: 0.429

Gnomad4 EAS AF: 0.538

Gnomad4 SAS AF: 0.411

Gnomad4 FIN AF: 0.436

Gnomad4 NFE AF: 0.376

Gnomad4 OTH AF: 0.420

Alfa AF: 0.391 Hom.: 14389

Bravo AF: 0.444

Asia WGS AF: 0.482 AC: 1675 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	0.69
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: rs10790218; hg19: chr11-117741995;