9-27386507-T-G

Variant names:

• chr9-27386507-T-G
• rs1110155
• NM_024761.5:c.419-27271A>C

Variant summary

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

The NM_024761.5(MOB3B):​c.419-27271A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.305 in 152,122 control chromosomes in the GnomAD database, including 8,239 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 0.30 (8239 hom., cov: 32)
• Consequence: MOB3B NM_024761.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.647
• Publications: 6 publications found

Genes affected

MOB3B (HGNC:23825): (MOB kinase activator 3B) The protein encoded by this gene shares similarity with the yeast Mob1 protein. Yeast Mob1 binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint regulation. This gene is located on the opposite strand as the interferon kappa precursor (IFNK) gene. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.767 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MOB3B	NM_024761.5	c.419-27271A>C		intron_variant	Intron 2 of 3	ENST00000262244.6	NP_079037.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MOB3B	ENST00000262244.6	c.419-27271A>C		intron_variant	Intron 2 of 3	1	NM_024761.5	ENSP00000262244.5
MOB3B	ENST00000603061.1	n.624-27271A>C		intron_variant	Intron 1 of 1	5

Frequencies

GnomAD3 genomes AF: 0.304 AC: 46253 AN: 152004 Hom.: 8213 Cov.: 32

Gnomad AFR AF: 0.329

Gnomad AMI AF: 0.243

Gnomad AMR AF: 0.372

Gnomad ASJ AF: 0.329

Gnomad EAS AF: 0.788

Gnomad SAS AF: 0.554

Gnomad FIN AF: 0.156

Gnomad MID AF: 0.383

Gnomad NFE AF: 0.242

Gnomad OTH AF: 0.320

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

GnomAD4 genome AF: 0.305 AC: 46323 AN: 152122 Hom.: 8239 Cov.: 32 AF XY: 0.309 AC XY: 22978 AN XY: 74372

African (AFR) AF: 0.329 AC: 13654 AN: 41486

American (AMR) AF: 0.372 AC: 5686 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.329 AC: 1143 AN: 3470

East Asian (EAS) AF: 0.788 AC: 4072 AN: 5170

South Asian (SAS) AF: 0.553 AC: 2663 AN: 4818

European-Finnish (FIN) AF: 0.156 AC: 1656 AN: 10604

Middle Eastern (MID) AF: 0.381 AC: 112 AN: 294

European-Non Finnish (NFE) AF: 0.242 AC: 16424 AN: 67982

Other (OTH) AF: 0.327 AC: 692 AN: 2114

Alfa AF: 0.279 Hom.: 21384

Bravo AF: 0.320

Asia WGS AF: 0.658 AC: 2284 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	1.3
DANN	Benign	0.50
PhyloP100		-0.65
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: rs1110155; hg19: chr9-27386505;