rs35668691

Variant names:

• chr10-96651536-G-A
• rs35668691
• NM_152309.3:c.828C>T

Variant summary

Our verdict is Benign. The variant received -19 ACMG points: 0P and 19B. BP4_Moderate BP6_Very_Strong BP7 BS1 BS2

The NM_152309.3(PIK3AP1):​c.828C>T​(p.Ala276Ala) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0289 in 1,614,100 control chromosomes in the GnomAD database, including 842 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.024 (62 hom., cov: 32)
  • Exomes 𝑓: 0.029 (780 hom.)
• Consequence: PIK3AP1 NM_152309.3 synonymous
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:2
• Conservation: PhyloP100: -0.753
• Publications: 5 publications found

Genes affected

PIK3AP1 (HGNC:30034): (phosphoinositide-3-kinase adaptor protein 1) Predicted to enable phosphatidylinositol 3-kinase regulatory subunit binding activity and signaling receptor binding activity. Predicted to be involved in regulation of inflammatory response; regulation of signal transduction; and toll-like receptor signaling pathway. Predicted to be located in cytoplasm and membrane. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -19 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.41).
• BP6: Variant 10-96651536-G-A is Benign according to our data. Variant chr10-96651536-G-A is described in ClinVar as Benign. ClinVar VariationId is 474932.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BP7: Synonymous conserved (PhyloP=-0.753 with no splicing effect.
• BS1: Variant frequency is greater than expected in population nfe. GnomAd4 allele frequency = 0.0236 (3600/152264) while in subpopulation NFE AF = 0.0343 (2332/68020). AF 95% confidence interval is 0.0331. There are 62 homozygotes in GnomAd4. There are 1755 alleles in the male GnomAd4 subpopulation. Median coverage is 32. This position passed quality control check.
• BS2: High AC in GnomAd4 at 3600 AD gene.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_152309.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PIK3AP1	NM_152309.3	MANE Select	c.828C>T	p.Ala276Ala	synonymous	Exon 5 of 17	NP_689522.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PIK3AP1	ENST00000339364.10	TSL:1 MANE Select	c.828C>T	p.Ala276Ala	synonymous	Exon 5 of 17	ENSP00000339826.5
	PIK3AP1	ENST00000371110.6	TSL:2	c.294C>T	p.Ala98Ala	synonymous	Exon 4 of 16	ENSP00000360151.2
	PIK3AP1	ENST00000468783.1	TSL:5	n.474C>T		non_coding_transcript_exon	Exon 4 of 8

Frequencies

GnomAD3 genomes AF: 0.0237 AC: 3603 AN: 152146 Hom.: 62 Cov.: 32

Gnomad AFR AF: 0.00541

Gnomad AMI AF: 0.0384

Gnomad AMR AF: 0.0268

Gnomad ASJ AF: 0.0297

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00580

Gnomad FIN AF: 0.0391

Gnomad MID AF: 0.0190

Gnomad NFE AF: 0.0343

Gnomad OTH AF: 0.0249

GnomAD2 exomes AF: 0.0256 AC: 6448 AN: 251400 AF XY: 0.0257

Gnomad AFR exome AF: 0.00394

Gnomad AMR exome AF: 0.0192

Gnomad ASJ exome AF: 0.0307

Gnomad EAS exome AF: 0.00

Gnomad FIN exome AF: 0.0383

Gnomad NFE exome AF: 0.0372

Gnomad OTH exome AF: 0.0300

GnomAD4 exome AF: 0.0295 AC: 43110 AN: 1461836 Hom.: 780 Cov.: 32 AF XY: 0.0291 AC XY: 21159 AN XY: 727208

African (AFR) AF: 0.00421 AC: 141 AN: 33480

American (AMR) AF: 0.0207 AC: 924 AN: 44724

Ashkenazi Jewish (ASJ) AF: 0.0295 AC: 772 AN: 26136

East Asian (EAS) AF: 0.0000252 AC: 1 AN: 39700

South Asian (SAS) AF: 0.00618 AC: 533 AN: 86256

European-Finnish (FIN) AF: 0.0406 AC: 2168 AN: 53416

Middle Eastern (MID) AF: 0.0342 AC: 197 AN: 5768

European-Non Finnish (NFE) AF: 0.0332 AC: 36871 AN: 1111964

Other (OTH) AF: 0.0249 AC: 1503 AN: 60392

GnomAD4 genome AF: 0.0236 AC: 3600 AN: 152264 Hom.: 62 Cov.: 32 AF XY: 0.0236 AC XY: 1755 AN XY: 74438

African (AFR) AF: 0.00539 AC: 224 AN: 41548

American (AMR) AF: 0.0267 AC: 408 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.0297 AC: 103 AN: 3472

East Asian (EAS) AF: 0.00 AC: 0 AN: 5186

South Asian (SAS) AF: 0.00559 AC: 27 AN: 4826

European-Finnish (FIN) AF: 0.0391 AC: 414 AN: 10598

Middle Eastern (MID) AF: 0.0170 AC: 5 AN: 294

European-Non Finnish (NFE) AF: 0.0343 AC: 2332 AN: 68020

Other (OTH) AF: 0.0246 AC: 52 AN: 2112

Alfa AF: 0.0324 Hom.: 323

Bravo AF: 0.0227

Asia WGS AF: 0.00318 AC: 11 AN: 3478

EpiCase AF: 0.0327

EpiControl AF: 0.0348

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

Infantile spasms Benign:1

Feb 03, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

not provided Benign:1

Breakthrough Genomics, Breakthrough Genomics

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: not provided

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.41
CADD	Benign	5.6
DANN	Benign	0.66
PhyloP100		-0.75
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: rs35668691; hg19: chr10-98411293;