NM_001017405.3:c.70-498G>A

Variant names:

• chr4-1311481-G-A
• rs6599300
• NM_001017405.3:c.70-498G>A

Variant summary

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

The NM_001017405.3(MAEA):​c.70-498G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.159 in 152,206 control chromosomes in the GnomAD database, including 3,721 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 0.16 (3721 hom., cov: 33)
• Consequence: MAEA NM_001017405.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.497
• Publications: 7 publications found

Genes affected

MAEA (HGNC:13731): (macrophage erythroblast attacher, E3 ubiquitin ligase) This gene encodes a protein that mediates the attachment of erythroblasts to macrophages. This attachment promotes terminal maturation and enucleation of erythroblasts, presumably by suppressing apoptosis. The encoded protein is an integral membrane protein with the N-terminus on the extracellular side and the C-terminus on the cytoplasmic side of the cell. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.404 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MAEA	NM_001017405.3	c.70-498G>A		intron_variant	Intron 1 of 8	ENST00000303400.9	NP_001017405.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MAEA	ENST00000303400.9	c.70-498G>A		intron_variant	Intron 1 of 8	1	NM_001017405.3	ENSP00000302830.4

Frequencies

GnomAD3 genomes AF: 0.159 AC: 24144 AN: 152088 Hom.: 3707 Cov.: 33

Gnomad AFR AF: 0.353

Gnomad AMI AF: 0.00329

Gnomad AMR AF: 0.246

Gnomad ASJ AF: 0.0674

Gnomad EAS AF: 0.418

Gnomad SAS AF: 0.157

Gnomad FIN AF: 0.0467

Gnomad MID AF: 0.0981

Gnomad NFE AF: 0.0270

Gnomad OTH AF: 0.128

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

GnomAD4 genome AF: 0.159 AC: 24204 AN: 152206 Hom.: 3721 Cov.: 33 AF XY: 0.162 AC XY: 12041 AN XY: 74440

African (AFR) AF: 0.353 AC: 14663 AN: 41480

American (AMR) AF: 0.247 AC: 3771 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.0674 AC: 234 AN: 3472

East Asian (EAS) AF: 0.418 AC: 2156 AN: 5154

South Asian (SAS) AF: 0.155 AC: 747 AN: 4832

European-Finnish (FIN) AF: 0.0467 AC: 496 AN: 10618

Middle Eastern (MID) AF: 0.0986 AC: 29 AN: 294

European-Non Finnish (NFE) AF: 0.0270 AC: 1836 AN: 68036

Other (OTH) AF: 0.127 AC: 269 AN: 2112

Alfa AF: 0.0705 Hom.: 2166

Bravo AF: 0.186

Asia WGS AF: 0.241 AC: 835 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.74
DANN	Benign	0.52
PhyloP100		-0.50
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs6599300; hg19: chr4-1305269;