NM_016281.4:c.1195-4276A>C

Variant names:

• chr12-118194217-T-G
• rs17512198
• NM_016281.4:c.1195-4276A>C

Variant summary

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

The NM_016281.4(TAOK3):​c.1195-4276A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.12 in 152,152 control chromosomes in the GnomAD database, including 1,195 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 0.12 (1195 hom., cov: 32)
• Consequence: TAOK3 NM_016281.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.954
• Publications: 2 publications found

Genes affected

TAOK3 (HGNC:18133): (TAO kinase 3) The protein encoded by this gene is a serine/threonine protein kinase that activates the p38/MAPK14 stress-activated MAPK cascade but inhibits the basal activity of the MAPK8/JNK cascade. The encoded protein is a member of the GCK subfamily of STE20-like kinases. [provided by RefSeq, Oct 2016]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.73).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.14 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_016281.4. 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
	TAOK3	NM_016281.4	MANE Select	c.1195-4276A>C		intron	N/A	NP_057365.3
	TAOK3	NM_001346487.2		c.1222-4276A>C		intron	N/A	NP_001333416.1
	TAOK3	NM_001346488.2		c.1195-4276A>C		intron	N/A	NP_001333417.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TAOK3	ENST00000392533.8	TSL:1 MANE Select	c.1195-4276A>C		intron	N/A	ENSP00000376317.3
	TAOK3	ENST00000419821.6	TSL:1	c.1195-4276A>C		intron	N/A	ENSP00000416374.2
	TAOK3	ENST00000537305.5	TSL:5	n.1876-4276A>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.120 AC: 18286 AN: 152034 Hom.: 1194 Cov.: 32

Gnomad AFR AF: 0.100

Gnomad AMI AF: 0.0625

Gnomad AMR AF: 0.105

Gnomad ASJ AF: 0.135

Gnomad EAS AF: 0.0106

Gnomad SAS AF: 0.0579

Gnomad FIN AF: 0.162

Gnomad MID AF: 0.166

Gnomad NFE AF: 0.143

Gnomad OTH AF: 0.103

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

GnomAD4 genome AF: 0.120 AC: 18285 AN: 152152 Hom.: 1195 Cov.: 32 AF XY: 0.118 AC XY: 8776 AN XY: 74374

African (AFR) AF: 0.0999 AC: 4145 AN: 41496

American (AMR) AF: 0.105 AC: 1602 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.135 AC: 470 AN: 3472

East Asian (EAS) AF: 0.0106 AC: 55 AN: 5180

South Asian (SAS) AF: 0.0588 AC: 283 AN: 4816

European-Finnish (FIN) AF: 0.162 AC: 1720 AN: 10588

Middle Eastern (MID) AF: 0.147 AC: 43 AN: 292

European-Non Finnish (NFE) AF: 0.143 AC: 9689 AN: 67990

Other (OTH) AF: 0.105 AC: 221 AN: 2114

Alfa AF: 0.131 Hom.: 218

Bravo AF: 0.113

Asia WGS AF: 0.0360 AC: 125 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.73
CADD	Benign	6.4
DANN	Benign	0.67
PhyloP100		0.95
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: rs17512198; hg19: chr12-118632022;