chr1-45912596-A-G

Variant names:

• chr1-45912596-A-G
• rs6686134
• NM_015112.3:c.500+30201A>G

Variant summary

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

The NM_015112.3(MAST2):​c.500+30201A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.445 in 151,998 control chromosomes in the GnomAD database, including 15,265 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 0.45 (15265 hom., cov: 32)
• Consequence: MAST2 NM_015112.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.211
• Publications: 7 publications found

Genes affected

MAST2 (HGNC:19035): (microtubule associated serine/threonine kinase 2) Enables phosphatase binding activity. Predicted to be involved in several processes, including peptidyl-serine phosphorylation; regulation of interleukin-12 production; and spermatid differentiation. Predicted to be located in cytoplasm and plasma membrane. Predicted to be active in microtubule cytoskeleton. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.611 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MAST2	NM_015112.3	c.500+30201A>G		intron_variant	Intron 4 of 28	ENST00000361297.7	NP_055927.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MAST2	ENST00000361297.7	c.500+30201A>G		intron_variant	Intron 4 of 28	1	NM_015112.3	ENSP00000354671.2
MAST2	ENST00000470809.1	n.470-4743A>G		intron_variant	Intron 4 of 4	3

Frequencies

GnomAD3 genomes AF: 0.446 AC: 67690 AN: 151880 Hom.: 15280 Cov.: 32

Gnomad AFR AF: 0.419

Gnomad AMI AF: 0.468

Gnomad AMR AF: 0.489

Gnomad ASJ AF: 0.467

Gnomad EAS AF: 0.630

Gnomad SAS AF: 0.448

Gnomad FIN AF: 0.412

Gnomad MID AF: 0.377

Gnomad NFE AF: 0.442

Gnomad OTH AF: 0.441

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

GnomAD4 genome AF: 0.445 AC: 67670 AN: 151998 Hom.: 15265 Cov.: 32 AF XY: 0.446 AC XY: 33121 AN XY: 74274

African (AFR) AF: 0.418 AC: 17321 AN: 41440

American (AMR) AF: 0.488 AC: 7464 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.467 AC: 1622 AN: 3472

East Asian (EAS) AF: 0.629 AC: 3249 AN: 5166

South Asian (SAS) AF: 0.446 AC: 2152 AN: 4820

European-Finnish (FIN) AF: 0.412 AC: 4349 AN: 10544

Middle Eastern (MID) AF: 0.371 AC: 109 AN: 294

European-Non Finnish (NFE) AF: 0.442 AC: 30061 AN: 67960

Other (OTH) AF: 0.435 AC: 919 AN: 2114

Alfa AF: 0.355 Hom.: 1368

Bravo AF: 0.449

Asia WGS AF: 0.520 AC: 1806 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	1.7
DANN	Benign	0.60
PhyloP100		-0.21
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: rs6686134; hg19: chr1-46378268;