rs353647

chr11-35169898-C-G

Variant summary

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

The NM_000610.4(CD44):c.68-6677C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.485 in 151,998 control chromosomes in the GnomAD database, including 18,268 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as association (no stars).

• Frequency: Genomes: 𝑓 0.49 (18268 hom., cov: 31)
• Consequence: CD44 NM_000610.4 intron
• Clinical Significance: association no assertion criteria provided O:1
• Conservation: PhyloP100: -0.833

Genes affected

CD44 (HGNC:1681): (CD44 molecule (IN blood group)) The protein encoded by this gene is a cell-surface glycoprotein involved in cell-cell interactions, cell adhesion and migration. It is a receptor for hyaluronic acid (HA) and can also interact with other ligands, such as osteopontin, collagens, and matrix metalloproteinases (MMPs). This protein participates in a wide variety of cellular functions including lymphocyte activation, recirculation and homing, hematopoiesis, and tumor metastasis. Transcripts for this gene undergo complex alternative splicing that results in many functionally distinct isoforms, however, the full length nature of some of these variants has not been determined. Alternative splicing is the basis for the structural and functional diversity of this protein, and may be related to tumor metastasis. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.543 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CD44	NM_000610.4	c.68-6677C>G		intron_variant		ENST00000428726.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CD44	ENST00000428726.8	c.68-6677C>G		intron_variant		1	NM_000610.4	A2

Frequencies

GnomAD3 genomes AF: 0.485 AC: 73632 AN: 151880 Hom.: 18221 Cov.: 31

Gnomad AFR AF: 0.541

Gnomad AMI AF: 0.499

Gnomad AMR AF: 0.552

Gnomad ASJ AF: 0.484

Gnomad EAS AF: 0.220

Gnomad SAS AF: 0.490

Gnomad FIN AF: 0.425

Gnomad MID AF: 0.487

Gnomad NFE AF: 0.465

Gnomad OTH AF: 0.495

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

GnomAD4 genome AF: 0.485 AC: 73743 AN: 151998 Hom.: 18268 Cov.: 31 AF XY: 0.485 AC XY: 36006 AN XY: 74292

Gnomad4 AFR AF: 0.541

Gnomad4 AMR AF: 0.552

Gnomad4 ASJ AF: 0.484

Gnomad4 EAS AF: 0.221

Gnomad4 SAS AF: 0.490

Gnomad4 FIN AF: 0.425

Gnomad4 NFE AF: 0.465

Gnomad4 OTH AF: 0.499

Alfa AF: 0.479 Hom.: 2219

Bravo AF: 0.492

Asia WGS AF: 0.412 AC: 1429 AN: 3478

ClinVar

Significance: association

Submissions summary: Other:1

Revision: no assertion criteria provided

Submissions by phenotype

Nephrolithiasis, calcium oxalate Other:1

association, no assertion criteria provided

case-control

Division of Molecular Genetics and Division of Molecular Medicine, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University

Mar 01, 2014

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
Cadd	Benign	0.10
Dann	Benign	0.46

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: rs353647; hg19: chr11-35191445;