chr1-171267187-T-C

Variant names:

• chr1-171267187-T-C
• rs16864296
• NM_001282693.2:c.133-356T>C

Variant summary

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

The NM_001282693.2(FMO1):​c.133-356T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0414 in 152,280 control chromosomes in the GnomAD database, including 173 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 0.041 (173 hom., cov: 32)
• Consequence: FMO1 NM_001282693.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.43
• Publications: 3 publications found

Genes affected

FMO1 (HGNC:3769): (flavin containing dimethylaniline monoxygenase 1) Metabolic N-oxidation of the diet-derived amino-trimethylamine (TMA) is mediated by flavin-containing monooxygenase and is subject to an inherited FMO3 polymorphism in man resulting in a small subpopulation with reduced TMA N-oxidation capacity resulting in fish odor syndrome Trimethylaminuria. Three forms of the enzyme, FMO1 found in fetal liver, FMO2 found in adult liver, and FMO3 are encoded by genes clustered in the 1q23-q25 region. Flavin-containing monooxygenases are NADPH-dependent flavoenzymes that catalyzes the oxidation of soft nucleophilic heteroatom centers in drugs, pesticides, and xenobiotics. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.062 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001282693.2. 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
	FMO1	NM_001282693.2	MANE Select	c.133-356T>C		intron	N/A	NP_001269622.1
	FMO1	NM_001282692.1		c.145-356T>C		intron	N/A	NP_001269621.1
	FMO1	NM_002021.3		c.133-356T>C		intron	N/A	NP_002012.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FMO1	ENST00000617670.6	TSL:1 MANE Select	c.133-356T>C		intron	N/A	ENSP00000481732.1
	FMO1	ENST00000354841.4	TSL:1	c.133-356T>C		intron	N/A	ENSP00000346901.4
	FMO1	ENST00000367750.7	TSL:1	c.133-356T>C		intron	N/A	ENSP00000356724.3

Frequencies

GnomAD3 genomes AF: 0.0415 AC: 6310 AN: 152162 Hom.: 173 Cov.: 32

Gnomad AFR AF: 0.0102

Gnomad AMI AF: 0.0504

Gnomad AMR AF: 0.0395

Gnomad ASJ AF: 0.0314

Gnomad EAS AF: 0.0675

Gnomad SAS AF: 0.0160

Gnomad FIN AF: 0.0602

Gnomad MID AF: 0.0380

Gnomad NFE AF: 0.0580

Gnomad OTH AF: 0.0502

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

GnomAD4 genome AF: 0.0414 AC: 6307 AN: 152280 Hom.: 173 Cov.: 32 AF XY: 0.0415 AC XY: 3092 AN XY: 74454

African (AFR) AF: 0.0102 AC: 424 AN: 41574

American (AMR) AF: 0.0394 AC: 603 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.0314 AC: 109 AN: 3472

East Asian (EAS) AF: 0.0678 AC: 351 AN: 5176

South Asian (SAS) AF: 0.0158 AC: 76 AN: 4812

European-Finnish (FIN) AF: 0.0602 AC: 639 AN: 10616

Middle Eastern (MID) AF: 0.0340 AC: 10 AN: 294

European-Non Finnish (NFE) AF: 0.0580 AC: 3944 AN: 68012

Other (OTH) AF: 0.0497 AC: 105 AN: 2114

Alfa AF: 0.0500 Hom.: 325

Bravo AF: 0.0396

Asia WGS AF: 0.0340 AC: 119 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	6.2
DANN	Benign	0.62
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: rs16864296; hg19: chr1-171236326;