rs1121980

Variant names:

• chr16-53775335-G-A
• rs1121980
• NM_001080432.3:c.46-34805G>A

Your query was ambiguous. Multiple possible variants found:

• chr16-53775335-G-A
• chr16-53775335-G-C
• chr16-53775335-G-T

Variant summary

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

The NM_001080432.3(FTO):​c.46-34805G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.432 in 151,826 control chromosomes in the GnomAD database, including 14,452 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 0.43 (14452 hom., cov: 31)
• Consequence: FTO NM_001080432.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.31

Genes affected

FTO (HGNC:24678): (FTO alpha-ketoglutarate dependent dioxygenase) This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA and RNA damage by oxidative demethylation. Studies in mice and humans indicate a role in nervous and cardiovascular systems and a strong association with body mass index, obesity risk, and type 2 diabetes. [provided by RefSeq, Jul 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.468 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FTO	NM_001080432.3	c.46-34805G>A		intron_variant	Intron 1 of 8	ENST00000471389.6	NP_001073901.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FTO	ENST00000471389.6	c.46-34805G>A		intron_variant	Intron 1 of 8	1	NM_001080432.3	ENSP00000418823.1

Frequencies

GnomAD3 genomes AF: 0.432 AC: 65558 AN: 151710 Hom.: 14437 Cov.: 31

Gnomad AFR AF: 0.473

Gnomad AMI AF: 0.485

Gnomad AMR AF: 0.355

Gnomad ASJ AF: 0.553

Gnomad EAS AF: 0.197

Gnomad SAS AF: 0.413

Gnomad FIN AF: 0.432

Gnomad MID AF: 0.418

Gnomad NFE AF: 0.437

Gnomad OTH AF: 0.429

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

GnomAD4 genome AF: 0.432 AC: 65609 AN: 151826 Hom.: 14452 Cov.: 31 AF XY: 0.429 AC XY: 31836 AN XY: 74152

Gnomad4 AFR AF: 0.473 AC: 0.473462 AN: 0.473462

Gnomad4 AMR AF: 0.356 AC: 0.355599 AN: 0.355599

Gnomad4 ASJ AF: 0.553 AC: 0.552768 AN: 0.552768

Gnomad4 EAS AF: 0.197 AC: 0.196588 AN: 0.196588

Gnomad4 SAS AF: 0.413 AC: 0.412682 AN: 0.412682

Gnomad4 FIN AF: 0.432 AC: 0.431866 AN: 0.431866

Gnomad4 NFE AF: 0.437 AC: 0.436786 AN: 0.436786

Gnomad4 OTH AF: 0.430 AC: 0.429725 AN: 0.429725

Alfa AF: 0.427 Hom.: 61902

Bravo AF: 0.422

Asia WGS AF: 0.342 AC: 1188 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	0.024
DANN	Benign	0.37
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

Publications

LitVar

Other links and lift over

dbSNP: rs1121980; hg19: chr16-53809247;