5-67017095-G-A

Variant names:

• chr5-67017095-G-A
• rs542778
• NM_001164664.2:c.675-37309G>A

Variant summary

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

The NM_001164664.2(MAST4):​c.675-37309G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.504 in 152,022 control chromosomes in the GnomAD database, including 20,557 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 (20557 hom., cov: 32)
• Consequence: MAST4 NM_001164664.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.403
• Publications: 2 publications found

Genes affected

MAST4 (HGNC:19037): (microtubule associated serine/threonine kinase family member 4) This gene encodes a member of the microtubule-associated serine/threonine protein kinases. The proteins in this family contain a domain that gives the kinase the ability to determine its own scaffold to control the effects of their kinase activities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.693 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MAST4	NM_001164664.2	c.675-37309G>A		intron_variant	Intron 4 of 28	ENST00000403625.7	NP_001158136.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MAST4	ENST00000403625.7	c.675-37309G>A		intron_variant	Intron 4 of 28	5	NM_001164664.2	ENSP00000385727.1

Frequencies

GnomAD3 genomes AF: 0.503 AC: 76460 AN: 151904 Hom.: 20508 Cov.: 32

Gnomad AFR AF: 0.699

Gnomad AMI AF: 0.281

Gnomad AMR AF: 0.515

Gnomad ASJ AF: 0.373

Gnomad EAS AF: 0.313

Gnomad SAS AF: 0.478

Gnomad FIN AF: 0.415

Gnomad MID AF: 0.421

Gnomad NFE AF: 0.422

Gnomad OTH AF: 0.495

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

GnomAD4 genome AF: 0.504 AC: 76570 AN: 152022 Hom.: 20557 Cov.: 32 AF XY: 0.502 AC XY: 37312 AN XY: 74288

African (AFR) AF: 0.699 AC: 29011 AN: 41474

American (AMR) AF: 0.515 AC: 7862 AN: 15264

Ashkenazi Jewish (ASJ) AF: 0.373 AC: 1294 AN: 3472

East Asian (EAS) AF: 0.314 AC: 1624 AN: 5170

South Asian (SAS) AF: 0.479 AC: 2304 AN: 4814

European-Finnish (FIN) AF: 0.415 AC: 4375 AN: 10542

Middle Eastern (MID) AF: 0.412 AC: 121 AN: 294

European-Non Finnish (NFE) AF: 0.422 AC: 28679 AN: 67966

Other (OTH) AF: 0.494 AC: 1044 AN: 2114

Alfa AF: 0.464 Hom.: 2177

Bravo AF: 0.515

Asia WGS AF: 0.431 AC: 1500 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	9.5
DANN	Benign	0.74
PhyloP100		0.40
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: rs542778; hg19: chr5-66312923;