chr15-55902679-T-C

Variant names:

• chr15-55902679-T-C
• rs8032158
• NM_006154.4:c.291+21967A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_006154.4(NEDD4):​c.291+21967A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.315 in 151,994 control chromosomes in the GnomAD database, including 7,665 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 0.31 (7665 hom., cov: 33)
• Consequence: NEDD4 NM_006154.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0480
• Publications: 45 publications found

Genes affected

NEDD4 (HGNC:7727): (NEDD4 E3 ubiquitin protein ligase) This gene is the founding member of the NEDD4 family of HECT ubiquitin ligases that function in the ubiquitin proteasome system of protein degradation. The encoded protein contains an N-terminal calcium and phospholipid binding C2 domain followed by multiple tryptophan-rich WW domains and, a C-terminal HECT ubiquitin ligase catalytic domain. It plays critical role in the regulation of a number of membrane receptors, endocytic machinery components and the tumor suppressor PTEN. [provided by RefSeq, Jul 2016]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.398 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006154.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NEDD4	NM_006154.4	MANE Select	c.291+21967A>G		intron	N/A	NP_006145.2	P46934-4
	NEDD4	NM_001284338.2		c.1548+12605A>G		intron	N/A	NP_001271267.1	P46934-1
	NEDD4	NM_001284339.1		c.1548+12605A>G		intron	N/A	NP_001271268.1	P46934-2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NEDD4	ENST00000435532.8	TSL:1 MANE Select	c.291+21967A>G		intron	N/A	ENSP00000410613.3	P46934-4
	NEDD4	ENST00000508342.5	TSL:1	c.1548+12605A>G		intron	N/A	ENSP00000424827.1	P46934-1
	NEDD4	ENST00000506154.1	TSL:1	c.1548+12605A>G		intron	N/A	ENSP00000422705.1	P46934-2

Frequencies

GnomAD3 genomes AF: 0.315 AC: 47807 AN: 151876 Hom.: 7667 Cov.: 33

Gnomad AFR AF: 0.304

Gnomad AMI AF: 0.307

Gnomad AMR AF: 0.322

Gnomad ASJ AF: 0.259

Gnomad EAS AF: 0.316

Gnomad SAS AF: 0.415

Gnomad FIN AF: 0.304

Gnomad MID AF: 0.312

Gnomad NFE AF: 0.318

Gnomad OTH AF: 0.297

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

GnomAD4 genome AF: 0.315 AC: 47822 AN: 151994 Hom.: 7665 Cov.: 33 AF XY: 0.317 AC XY: 23518 AN XY: 74278

African (AFR) AF: 0.303 AC: 12575 AN: 41450

American (AMR) AF: 0.321 AC: 4910 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.259 AC: 897 AN: 3470

East Asian (EAS) AF: 0.316 AC: 1637 AN: 5182

South Asian (SAS) AF: 0.413 AC: 1991 AN: 4816

European-Finnish (FIN) AF: 0.304 AC: 3198 AN: 10520

Middle Eastern (MID) AF: 0.322 AC: 94 AN: 292

European-Non Finnish (NFE) AF: 0.318 AC: 21617 AN: 67968

Other (OTH) AF: 0.297 AC: 624 AN: 2102

Alfa AF: 0.316 Hom.: 13016

Bravo AF: 0.309

Asia WGS AF: 0.356 AC: 1240 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	1.3
DANN	Benign	0.65
PhyloP100		0.048
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs8032158; hg19: chr15-56194877;