rs11938298

chr4-143587655-C-Gchr4-143587655-C-T

Variant summary

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

The NM_001168235.2(FREM3):c.6029-1662G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.709 in 152,022 control chromosomes in the GnomAD database, including 40,211 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 0.71 (40211 hom., cov: 31)
• Consequence: FREM3 NM_001168235.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.49

Genes affected

FREM3 (HGNC:25172): (FRAS1 related extracellular matrix 3) This gene encodes an integral membrane protein containing numerous CSPG (chondroitin sulfate proteoglycan element) repeats and Calx-beta domains. The protein belongs to the family of FRAS1/FREM extracellular matrix proteins and may play a role cell adhesion. [provided by RefSeq, Feb 2017]

GUSBP5 (HGNC:42319): (GUSB pseudogene 5)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.826 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FREM3	NM_001168235.2	c.6029-1662G>C		intron_variant		ENST00000329798.5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FREM3	ENST00000329798.5	c.6029-1662G>C		intron_variant		5	NM_001168235.2	P1
GUSBP5	ENST00000641328.1	n.861+15074C>G		intron_variant, non_coding_transcript_variant
GUSBP5	ENST00000511042.5	n.191+15074C>G		intron_variant, non_coding_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.709 AC: 107699 AN: 151906 Hom.: 40196 Cov.: 31

Gnomad AFR AF: 0.527

Gnomad AMI AF: 0.885

Gnomad AMR AF: 0.717

Gnomad ASJ AF: 0.826

Gnomad EAS AF: 0.219

Gnomad SAS AF: 0.669

Gnomad FIN AF: 0.813

Gnomad MID AF: 0.782

Gnomad NFE AF: 0.832

Gnomad OTH AF: 0.737

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

GnomAD4 genome AF: 0.709 AC: 107748 AN: 152022 Hom.: 40211 Cov.: 31 AF XY: 0.704 AC XY: 52299 AN XY: 74320

Gnomad4 AFR AF: 0.527

Gnomad4 AMR AF: 0.717

Gnomad4 ASJ AF: 0.826

Gnomad4 EAS AF: 0.220

Gnomad4 SAS AF: 0.669

Gnomad4 FIN AF: 0.813

Gnomad4 NFE AF: 0.832

Gnomad4 OTH AF: 0.732

Alfa AF: 0.762 Hom.: 5622

Bravo AF: 0.694

Asia WGS AF: 0.478 AC: 1661 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
Cadd	Benign	2.9
Dann	Benign	0.63

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: rs11938298; hg19: chr4-144508808;