chr8-9584517-A-C

Variant names:

• chr8-9584517-A-C
• rs12549064
• NM_003747.3:c.898+4134A>C

Variant summary

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

The NM_003747.3(TNKS):​c.898+4134A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.177 in 151,948 control chromosomes in the GnomAD database, including 2,598 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 0.18 (2598 hom., cov: 32)
• Consequence: TNKS NM_003747.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.712
• Publications: 9 publications found

Genes affected

TNKS (HGNC:11941): (tankyrase) Enables histone binding activity; pentosyltransferase activity; and zinc ion binding activity. Involved in several processes, including negative regulation of maintenance of mitotic sister chromatid cohesion, telomeric; protein ADP-ribosylation; and regulation of nucleobase-containing compound metabolic process. Acts upstream of or within peptidyl-serine phosphorylation; peptidyl-threonine phosphorylation; and protein ADP-ribosylation. Located in several cellular components, including chromosome, telomeric region; mitotic spindle pole; and nucleus. [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=-1.02).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.296 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_003747.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TNKS	NM_003747.3	MANE Select	c.898+4134A>C		intron	N/A	NP_003738.2	O95271-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TNKS	ENST00000310430.11	TSL:1 MANE Select	c.898+4134A>C		intron	N/A	ENSP00000311579.6	O95271-1
	TNKS	ENST00000517770.2	TSL:4	c.898+4134A>C		intron	N/A	ENSP00000428185.2	H0YAW5
	TNKS	ENST00000885812.1		c.898+4134A>C		intron	N/A	ENSP00000555871.1

Frequencies

GnomAD3 genomes AF: 0.177 AC: 26867 AN: 151830 Hom.: 2595 Cov.: 32

Gnomad AFR AF: 0.171

Gnomad AMI AF: 0.190

Gnomad AMR AF: 0.114

Gnomad ASJ AF: 0.0889

Gnomad EAS AF: 0.308

Gnomad SAS AF: 0.136

Gnomad FIN AF: 0.301

Gnomad MID AF: 0.114

Gnomad NFE AF: 0.174

Gnomad OTH AF: 0.147

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

GnomAD4 genome AF: 0.177 AC: 26886 AN: 151948 Hom.: 2598 Cov.: 32 AF XY: 0.179 AC XY: 13294 AN XY: 74242

African (AFR) AF: 0.171 AC: 7096 AN: 41410

American (AMR) AF: 0.113 AC: 1733 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.0889 AC: 308 AN: 3466

East Asian (EAS) AF: 0.309 AC: 1594 AN: 5164

South Asian (SAS) AF: 0.135 AC: 648 AN: 4806

European-Finnish (FIN) AF: 0.301 AC: 3178 AN: 10548

Middle Eastern (MID) AF: 0.119 AC: 35 AN: 294

European-Non Finnish (NFE) AF: 0.174 AC: 11813 AN: 67960

Other (OTH) AF: 0.146 AC: 308 AN: 2110

Alfa AF: 0.161 Hom.: 3626

Bravo AF: 0.167

Asia WGS AF: 0.203 AC: 706 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.27
DANN	Benign	0.44
PhyloP100		-0.71
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: rs12549064; hg19: chr8-9442027;