rs10492629

Positions:

• chr13-94384899-T-C

Variant summary

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

The NM_005708.5(GPC6):​c.1289+2349T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.136 in 152,166 control chromosomes in the GnomAD database, including 1,596 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 0.14 (1596 hom., cov: 32)
• Consequence: GPC6 NM_005708.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.383

Genes affected

GPC6 (HGNC:4454): (glypican 6) The glypicans comprise a family of glycosylphosphatidylinositol-anchored heparan sulfate proteoglycans, and they have been implicated in the control of cell growth and cell division. The glypican encoded by this gene is a putative cell surface coreceptor for growth factors, extracellular matrix proteins, proteases and anti-proteases. Mutations in this gene are associated with omodysplasia 1. [provided by RefSeq, Nov 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.27 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
GPC6	NM_005708.5	c.1289+2349T>C		intron_variant		ENST00000377047.9	NP_005699.1
GPC6	XM_017020300.2	c.1079+2349T>C		intron_variant			XP_016875789.1
GPC6	XM_017020302.2	c.596+2349T>C		intron_variant			XP_016875791.1
GPC6	XM_047429990.1	c.1079+2349T>C		intron_variant			XP_047285946.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
GPC6	ENST00000377047.9	c.1289+2349T>C		intron_variant		1	NM_005708.5	ENSP00000366246	P1

Frequencies

GnomAD3 genomes AF: 0.136 AC: 20675 AN: 152048 Hom.: 1596 Cov.: 32

Gnomad AFR AF: 0.0961

Gnomad AMI AF: 0.0822

Gnomad AMR AF: 0.109

Gnomad ASJ AF: 0.0781

Gnomad EAS AF: 0.282

Gnomad SAS AF: 0.225

Gnomad FIN AF: 0.104

Gnomad MID AF: 0.0728

Gnomad NFE AF: 0.159

Gnomad OTH AF: 0.103

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

GnomAD4 genome AF: 0.136 AC: 20690 AN: 152166 Hom.: 1596 Cov.: 32 AF XY: 0.135 AC XY: 10008 AN XY: 74386

Gnomad4 AFR AF: 0.0961

Gnomad4 AMR AF: 0.109

Gnomad4 ASJ AF: 0.0781

Gnomad4 EAS AF: 0.282

Gnomad4 SAS AF: 0.224

Gnomad4 FIN AF: 0.104

Gnomad4 NFE AF: 0.159

Gnomad4 OTH AF: 0.109

Alfa AF: 0.154 Hom.: 1198

Bravo AF: 0.132

Asia WGS AF: 0.217 AC: 755 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	1.1
DANN	Benign	0.70

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: rs10492629; hg19: chr13-95037153;