rs2855025

Variant names:

• chr10-69096216-A-T
• rs2855025
• NM_002727.4:c.80-868A>T

Variant summary

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

The NM_002727.4(SRGN):​c.80-868A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.418 in 151,950 control chromosomes in the GnomAD database, including 15,275 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 0.42 (15275 hom., cov: 32)
• Consequence: SRGN NM_002727.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.957
• Publications: 4 publications found

Genes affected

SRGN (HGNC:9361): (serglycin) This gene encodes a protein best known as a hematopoietic cell granule proteoglycan. Proteoglycans stored in the secretory granules of many hematopoietic cells also contain a protease-resistant peptide core, which may be important for neutralizing hydrolytic enzymes. This encoded protein was found to be associated with the macromolecular complex of granzymes and perforin, which may serve as a mediator of granule-mediated apoptosis. Two transcript variants, only one of them protein-coding, have been found for this gene. [provided by RefSeq, Jul 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.531 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002727.4. 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
	SRGN	NM_002727.4	MANE Select	c.80-868A>T		intron	N/A	NP_002718.2
	SRGN	NM_001321053.2		c.80-868A>T		intron	N/A	NP_001307982.1
	SRGN	NM_001321054.1		c.60-7655A>T		intron	N/A	NP_001307983.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SRGN	ENST00000242465.4	TSL:1 MANE Select	c.80-868A>T		intron	N/A	ENSP00000242465.3
	SRGN	ENST00000718456.1		c.80-868A>T		intron	N/A	ENSP00000520834.1
	SRGN	ENST00000462445.1	TSL:2	n.132-7655A>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.419 AC: 63558 AN: 151832 Hom.: 15286 Cov.: 32

Gnomad AFR AF: 0.171

Gnomad AMI AF: 0.552

Gnomad AMR AF: 0.451

Gnomad ASJ AF: 0.689

Gnomad EAS AF: 0.398

Gnomad SAS AF: 0.460

Gnomad FIN AF: 0.457

Gnomad MID AF: 0.659

Gnomad NFE AF: 0.536

Gnomad OTH AF: 0.489

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

GnomAD4 genome AF: 0.418 AC: 63547 AN: 151950 Hom.: 15275 Cov.: 32 AF XY: 0.417 AC XY: 30967 AN XY: 74258

African (AFR) AF: 0.171 AC: 7068 AN: 41434

American (AMR) AF: 0.451 AC: 6877 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.689 AC: 2392 AN: 3472

East Asian (EAS) AF: 0.398 AC: 2056 AN: 5168

South Asian (SAS) AF: 0.460 AC: 2215 AN: 4816

European-Finnish (FIN) AF: 0.457 AC: 4816 AN: 10528

Middle Eastern (MID) AF: 0.651 AC: 190 AN: 292

European-Non Finnish (NFE) AF: 0.536 AC: 36402 AN: 67960

Other (OTH) AF: 0.486 AC: 1028 AN: 2116

Alfa AF: 0.478 Hom.: 2335

Bravo AF: 0.406

Asia WGS AF: 0.404 AC: 1404 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	0.41
DANN	Benign	0.65
PhyloP100		-0.96
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: rs2855025; hg19: chr10-70855972;