chr3-169494579-T-G

Position:

• chr3-169494579-T-G

Variant summary

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

The NM_004991.4(MECOM):​c.38-113055A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.817 in 152,144 control chromosomes in the GnomAD database, including 52,498 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 0.82 (52498 hom., cov: 32)
• Consequence: MECOM NM_004991.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.253

Genes affected

MECOM (HGNC:3498): (MDS1 and EVI1 complex locus) The protein encoded by this gene is a transcriptional regulator and oncoprotein that may be involved in hematopoiesis, apoptosis, development, and cell differentiation and proliferation. The encoded protein can interact with CTBP1, SMAD3, CREBBP, KAT2B, MAPK8, and MAPK9. This gene can undergo translocation with the AML1 gene, resulting in overexpression of this gene and the onset of leukemia. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]

MECOM (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.921 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MECOM	NM_004991.4	c.38-113055A>C		intron_variant		ENST00000651503.2	NP_004982.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MECOM	ENST00000651503.2	c.38-113055A>C		intron_variant			NM_004991.4	ENSP00000498411.1
MECOM	ENST00000485957.1	n.284-113055A>C		intron_variant		1
MECOM	ENST00000494292.6	c.38-113055A>C		intron_variant		5		ENSP00000417899.1
MECOM	ENST00000486748.2	c.109+71390A>C		intron_variant		5		ENSP00000419537.1

Frequencies

GnomAD3 genomes AF: 0.817 AC: 124268 AN: 152026 Hom.: 52494 Cov.: 32

Gnomad AFR AF: 0.579

Gnomad AMI AF: 0.940

Gnomad AMR AF: 0.843

Gnomad ASJ AF: 0.871

Gnomad EAS AF: 0.907

Gnomad SAS AF: 0.943

Gnomad FIN AF: 0.950

Gnomad MID AF: 0.870

Gnomad NFE AF: 0.915

Gnomad OTH AF: 0.833

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

GnomAD4 genome AF: 0.817 AC: 124304 AN: 152144 Hom.: 52498 Cov.: 32 AF XY: 0.823 AC XY: 61201 AN XY: 74392

Gnomad4 AFR AF: 0.579

Gnomad4 AMR AF: 0.843

Gnomad4 ASJ AF: 0.871

Gnomad4 EAS AF: 0.907

Gnomad4 SAS AF: 0.943

Gnomad4 FIN AF: 0.950

Gnomad4 NFE AF: 0.915

Gnomad4 OTH AF: 0.833

Alfa AF: 0.890 Hom.: 92630

Bravo AF: 0.797

Asia WGS AF: 0.891 AC: 3099 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	2.3
DANN	Benign	0.49

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs7638569; hg19: chr3-169212367;