chr2-85540612-C-T

Position:

• chr2-85540612-C-T

Variant summary

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

The NM_005911.6(MAT2A):​c.92-471C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.497 in 152,082 control chromosomes in the GnomAD database, including 19,953 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 0.50 (19953 hom., cov: 33)
• Consequence: MAT2A NM_005911.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.380

Genes affected

MAT2A (HGNC:6904): (methionine adenosyltransferase 2A) The protein encoded by this gene catalyzes the production of S-adenosylmethionine (AdoMet) from methionine and ATP. AdoMet is the key methyl donor in cellular processes. [provided by RefSeq, Jun 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.674 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MAT2A	NM_005911.6	c.92-471C>T		intron_variant		ENST00000306434.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MAT2A	ENST00000306434.8	c.92-471C>T		intron_variant		1	NM_005911.6	P1

Frequencies

GnomAD3 genomes AF: 0.497 AC: 75517 AN: 151964 Hom.: 19913 Cov.: 33

Gnomad AFR AF: 0.680

Gnomad AMI AF: 0.443

Gnomad AMR AF: 0.400

Gnomad ASJ AF: 0.387

Gnomad EAS AF: 0.390

Gnomad SAS AF: 0.376

Gnomad FIN AF: 0.417

Gnomad MID AF: 0.424

Gnomad NFE AF: 0.444

Gnomad OTH AF: 0.487

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

GnomAD4 genome AF: 0.497 AC: 75611 AN: 152082 Hom.: 19953 Cov.: 33 AF XY: 0.493 AC XY: 36676 AN XY: 74344

Gnomad4 AFR AF: 0.680

Gnomad4 AMR AF: 0.399

Gnomad4 ASJ AF: 0.387

Gnomad4 EAS AF: 0.390

Gnomad4 SAS AF: 0.376

Gnomad4 FIN AF: 0.417

Gnomad4 NFE AF: 0.444

Gnomad4 OTH AF: 0.489

Alfa AF: 0.446 Hom.: 22723

Bravo AF: 0.503

Asia WGS AF: 0.428 AC: 1492 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	4.9
DANN	Benign	0.52

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: rs2028900; hg19: chr2-85767735;