chr11-18269774-T-C

Variant names:

• chr11-18269774-T-C
• rs12218
• NM_199161.5:c.288T>C

Variant summary

Our verdict is Benign. The variant received -13 ACMG points: 0P and 13B. BP4_Strong BP7 BA1

The NM_199161.5(SAA1):​c.288T>C​(p.Ala96Ala) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.479 in 1,613,852 control chromosomes in the GnomAD database, including 195,674 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 0.37 (12485 hom., cov: 32)
  • Exomes 𝑓: 0.49 (183189 hom.)
• Consequence: SAA1 NM_199161.5 synonymous
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.40
• Publications: 50 publications found

Genes affected

SAA1 (HGNC:10513): (serum amyloid A1) This gene encodes a member of the serum amyloid A family of apolipoproteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a major acute phase protein that is highly expressed in response to inflammation and tissue injury. This protein also plays an important role in HDL metabolism and cholesterol homeostasis. High levels of this protein are associated with chronic inflammatory diseases including atherosclerosis, rheumatoid arthritis, Alzheimer's disease and Crohn's disease. This protein may also be a potential biomarker for certain tumors. Finally, antimicrobial activity against S. aureus and E. coli resides in the N-terminal portion of the mature protein. Alternate splicing results in multiple transcript variants that encode the same protein. A pseudogene of this gene is found on chromosome 11. [provided by RefSeq, Jul 2020]

ENSG00000303304 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -13 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BP7: Synonymous conserved (PhyloP=-1.4 with no splicing effect.
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.5 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_199161.5. 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
	SAA1	NM_199161.5	MANE Select	c.288T>C	p.Ala96Ala	synonymous	Exon 4 of 4	NP_954630.2	P0DJI8
	SAA1	NM_000331.6		c.288T>C	p.Ala96Ala	synonymous	Exon 4 of 4	NP_000322.3
	SAA1	NM_001178006.3		c.288T>C	p.Ala96Ala	synonymous	Exon 5 of 5	NP_001171477.2	P0DJI8

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SAA1	ENST00000356524.9	TSL:1 MANE Select	c.288T>C	p.Ala96Ala	synonymous	Exon 4 of 4	ENSP00000348918.4	P0DJI8
	SAA1	ENST00000532858.5	TSL:1	c.288T>C	p.Ala96Ala	synonymous	Exon 5 of 5	ENSP00000436866.1	P0DJI8
	SAA1	ENST00000405158.2	TSL:5	c.288T>C	p.Ala96Ala	synonymous	Exon 4 of 4	ENSP00000384906.2	P0DJI8

Frequencies

GnomAD3 genomes AF: 0.367 AC: 55743 AN: 152040 Hom.: 12486 Cov.: 32

Gnomad AFR AF: 0.105

Gnomad AMI AF: 0.466

Gnomad AMR AF: 0.434

Gnomad ASJ AF: 0.325

Gnomad EAS AF: 0.310

Gnomad SAS AF: 0.372

Gnomad FIN AF: 0.442

Gnomad MID AF: 0.294

Gnomad NFE AF: 0.504

Gnomad OTH AF: 0.373

GnomAD2 exomes AF: 0.417 AC: 104900 AN: 251420 AF XY: 0.420

Gnomad AFR exome AF: 0.0975

Gnomad AMR exome AF: 0.428

Gnomad ASJ exome AF: 0.313

Gnomad EAS exome AF: 0.301

Gnomad FIN exome AF: 0.446

Gnomad NFE exome AF: 0.494

Gnomad OTH exome AF: 0.432

GnomAD4 exome AF: 0.491 AC: 717446 AN: 1461692 Hom.: 183189 Cov.: 50 AF XY: 0.486 AC XY: 353386 AN XY: 727150

African (AFR) AF: 0.0849 AC: 2841 AN: 33474

American (AMR) AF: 0.433 AC: 19352 AN: 44716

Ashkenazi Jewish (ASJ) AF: 0.316 AC: 8246 AN: 26130

East Asian (EAS) AF: 0.309 AC: 12266 AN: 39700

South Asian (SAS) AF: 0.369 AC: 31835 AN: 86252

European-Finnish (FIN) AF: 0.451 AC: 24068 AN: 53416

Middle Eastern (MID) AF: 0.260 AC: 1501 AN: 5764

European-Non Finnish (NFE) AF: 0.531 AC: 590238 AN: 1111856

Other (OTH) AF: 0.449 AC: 27099 AN: 60384

GnomAD4 genome AF: 0.366 AC: 55749 AN: 152160 Hom.: 12485 Cov.: 32 AF XY: 0.364 AC XY: 27056 AN XY: 74386

African (AFR) AF: 0.104 AC: 4331 AN: 41534

American (AMR) AF: 0.435 AC: 6649 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.325 AC: 1127 AN: 3466

East Asian (EAS) AF: 0.310 AC: 1604 AN: 5166

South Asian (SAS) AF: 0.374 AC: 1803 AN: 4818

European-Finnish (FIN) AF: 0.442 AC: 4682 AN: 10594

Middle Eastern (MID) AF: 0.296 AC: 87 AN: 294

European-Non Finnish (NFE) AF: 0.504 AC: 34264 AN: 67970

Other (OTH) AF: 0.368 AC: 777 AN: 2110

Alfa AF: 0.428 Hom.: 6681

Bravo AF: 0.355

Asia WGS AF: 0.331 AC: 1151 AN: 3478

EpiCase AF: 0.477

EpiControl AF: 0.470

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	0.34
DANN	Benign	0.50
PhyloP100		-1.4
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: rs12218; hg19: chr11-18291321; COSMIC: COSV62946044; COSMIC: COSV62946044;