NM_014840.3:c.240+2031G>A

Variant names:

• chr12-106136383-C-T
• rs2559602
• NM_014840.3:c.240+2031G>A

Variant summary

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

The NM_014840.3(NUAK1):​c.240+2031G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.441 in 151,906 control chromosomes in the GnomAD database, including 16,215 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 0.44 (16215 hom., cov: 32)
• Consequence: NUAK1 NM_014840.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.00100
• Publications: 1 publications found

Genes affected

NUAK1 (HGNC:14311): (NUAK family kinase 1) Enables p53 binding activity and protein serine/threonine kinase activity. Involved in several processes, including protein phosphorylation; regulation of cellular senescence; and regulation of myosin-light-chain-phosphatase activity. Located in cytoplasm; microtubule cytoskeleton; and nuclear lumen. [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=-0.87).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.529 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_014840.3. 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
	NUAK1	NM_014840.3	MANE Select	c.240+2031G>A		intron	N/A	NP_055655.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NUAK1	ENST00000261402.7	TSL:1 MANE Select	c.240+2031G>A		intron	N/A	ENSP00000261402.2

Frequencies

GnomAD3 genomes AF: 0.442 AC: 67032 AN: 151788 Hom.: 16217 Cov.: 32

Gnomad AFR AF: 0.233

Gnomad AMI AF: 0.515

Gnomad AMR AF: 0.519

Gnomad ASJ AF: 0.491

Gnomad EAS AF: 0.435

Gnomad SAS AF: 0.548

Gnomad FIN AF: 0.598

Gnomad MID AF: 0.383

Gnomad NFE AF: 0.517

Gnomad OTH AF: 0.450

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

GnomAD4 genome AF: 0.441 AC: 67055 AN: 151906 Hom.: 16215 Cov.: 32 AF XY: 0.447 AC XY: 33212 AN XY: 74234

African (AFR) AF: 0.233 AC: 9631 AN: 41414

American (AMR) AF: 0.519 AC: 7928 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.491 AC: 1706 AN: 3472

East Asian (EAS) AF: 0.434 AC: 2237 AN: 5150

South Asian (SAS) AF: 0.547 AC: 2629 AN: 4808

European-Finnish (FIN) AF: 0.598 AC: 6309 AN: 10554

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

European-Non Finnish (NFE) AF: 0.517 AC: 35089 AN: 67926

Other (OTH) AF: 0.451 AC: 949 AN: 2104

Alfa AF: 0.487 Hom.: 68756

Bravo AF: 0.423

Asia WGS AF: 0.494 AC: 1719 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	3.5
DANN	Benign	0.65
PhyloP100		0.0010
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.050		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: rs2559602; hg19: chr12-106530161;