NM_001395430.1:c.-117-3180C>T

Variant names:

• chr15-40249998-C-T
• rs2277562
• NM_001395430.1:c.-117-3180C>T

Variant summary

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

The NM_001395430.1(PAK6):​c.-117-3180C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.148 in 152,290 control chromosomes in the GnomAD database, including 2,093 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 0.15 (2093 hom., cov: 33)
• Consequence: PAK6 NM_001395430.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.862
• Publications: 5 publications found

Genes affected

PAK6 (HGNC:16061): (p21 (RAC1) activated kinase 6) This gene encodes a member of a family of p21-stimulated serine/threonine protein kinases, which contain an amino-terminal Cdc42/Rac interactive binding (CRIB) domain and a carboxyl-terminal kinase domain. These kinases function in a number of cellular processes, including cytoskeleton rearrangement, apoptosis, and the mitogen-activated protein (MAP) kinase signaling pathway. The protein encoded by this gene interacts with androgen receptor (AR) and translocates to the nucleus, where it is involved in transcriptional regulation. Changes in expression of this gene have been linked to prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

BUB1B-PAK6 (HGNC:52276): (BUB1B-PAK6 readthrough) This gene represents readthrough transcription between the genes BUB1B (mitotic checkpoint serine/threonine-protein kinase BUB1 beta) and PAK6 (serine/threonine-protein kinase PAK 6). The protein encoded by the readthrough transcripts is the same as the product of the downstream gene (PAK6). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

ENSG00000299376 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.66).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.218 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001395430.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PAK6	NM_001395430.1	MANE Select	c.-117-3180C>T		intron	N/A	NP_001382359.1
	BUB1B-PAK6	NM_001128628.3		c.-117-3180C>T		intron	N/A	NP_001122100.1
	BUB1B-PAK6	NM_001128629.3		c.-117-3180C>T		intron	N/A	NP_001122101.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PAK6	ENST00000560346.6	TSL:5 MANE Select	c.-117-3180C>T		intron	N/A	ENSP00000453858.1
	PAK6	ENST00000260404.8	TSL:1	c.-117-3180C>T		intron	N/A	ENSP00000260404.4
	BUB1B-PAK6	ENST00000559435.1	TSL:5	n.300-3180C>T		intron	N/A	ENSP00000457109.1

Frequencies

GnomAD3 genomes AF: 0.148 AC: 22592 AN: 152172 Hom.: 2096 Cov.: 33

Gnomad AFR AF: 0.0412

Gnomad AMI AF: 0.357

Gnomad AMR AF: 0.143

Gnomad ASJ AF: 0.220

Gnomad EAS AF: 0.101

Gnomad SAS AF: 0.230

Gnomad FIN AF: 0.176

Gnomad MID AF: 0.288

Gnomad NFE AF: 0.201

Gnomad OTH AF: 0.157

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

GnomAD4 genome AF: 0.148 AC: 22573 AN: 152290 Hom.: 2093 Cov.: 33 AF XY: 0.149 AC XY: 11118 AN XY: 74464

African (AFR) AF: 0.0411 AC: 1711 AN: 41580

American (AMR) AF: 0.143 AC: 2189 AN: 15306

Ashkenazi Jewish (ASJ) AF: 0.220 AC: 764 AN: 3472

East Asian (EAS) AF: 0.101 AC: 522 AN: 5182

South Asian (SAS) AF: 0.229 AC: 1107 AN: 4824

European-Finnish (FIN) AF: 0.176 AC: 1873 AN: 10614

Middle Eastern (MID) AF: 0.279 AC: 82 AN: 294

European-Non Finnish (NFE) AF: 0.201 AC: 13673 AN: 67994

Other (OTH) AF: 0.154 AC: 326 AN: 2112

Alfa AF: 0.187 Hom.: 5764

Bravo AF: 0.137

Asia WGS AF: 0.148 AC: 515 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.66
CADD	Benign	18
DANN	Benign	0.80
PhyloP100		0.86
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: rs2277562; hg19: chr15-40542199;