3-167810341-T-C

Position:

• chr3-167810341-T-C

Variant summary

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

The NM_001122752.2(SERPINI1):​c.979+3000T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.544 in 151,844 control chromosomes in the GnomAD database, including 24,492 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 0.54 (24492 hom., cov: 31)
• Consequence: SERPINI1 NM_001122752.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.31

Genes affected

SERPINI1 (HGNC:8943): (serpin family I member 1) This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The protein is primarily secreted by axons in the brain, and preferentially reacts with and inhibits tissue-type plasminogen activator. It is thought to play a role in the regulation of axonal growth and the development of synaptic plasticity. Mutations in this gene result in familial encephalopathy with neuroserpin inclusion bodies (FENIB), which is a dominantly inherited form of familial encephalopathy and epilepsy characterized by the accumulation of mutant neuroserpin polymers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]

SERPINI1 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.749 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SERPINI1	NM_001122752.2	c.979+3000T>C		intron_variant		ENST00000446050.7	NP_001116224.1
SERPINI1	NM_005025.5	c.979+3000T>C		intron_variant			NP_005016.1
SERPINI1	XM_017006618.3	c.979+3000T>C		intron_variant			XP_016862107.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SERPINI1	ENST00000446050.7	c.979+3000T>C		intron_variant		1	NM_001122752.2	ENSP00000397373.2

Frequencies

GnomAD3 genomes AF: 0.543 AC: 82456 AN: 151726 Hom.: 24459 Cov.: 31

Gnomad AFR AF: 0.756

Gnomad AMI AF: 0.442

Gnomad AMR AF: 0.425

Gnomad ASJ AF: 0.472

Gnomad EAS AF: 0.0748

Gnomad SAS AF: 0.290

Gnomad FIN AF: 0.468

Gnomad MID AF: 0.430

Gnomad NFE AF: 0.512

Gnomad OTH AF: 0.531

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

GnomAD4 genome AF: 0.544 AC: 82535 AN: 151844 Hom.: 24492 Cov.: 31 AF XY: 0.532 AC XY: 39460 AN XY: 74196

Gnomad4 AFR AF: 0.756

Gnomad4 AMR AF: 0.425

Gnomad4 ASJ AF: 0.472

Gnomad4 EAS AF: 0.0745

Gnomad4 SAS AF: 0.289

Gnomad4 FIN AF: 0.468

Gnomad4 NFE AF: 0.512

Gnomad4 OTH AF: 0.528

Alfa AF: 0.508 Hom.: 11613

Bravo AF: 0.551

Asia WGS AF: 0.232 AC: 806 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	15
DANN	Benign	0.91

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: rs6783981; hg19: chr3-167528129;