chr15-72253535-T-C

Variant names:

• chr15-72253535-T-C
• rs1426166
• NM_001323532.2:c.1192-31A>G

Variant summary

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

The NM_001323532.2(PARP6):​c.1192-31A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 1 in 1,586,508 control chromosomes in the GnomAD database, including 792,845 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 1.0 (75956 hom., cov: 31)
  • Exomes 𝑓: 1.0 (716889 hom.)
• Consequence: PARP6 NM_001323532.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.71
• Publications: 7 publications found

Genes affected

PARP6 (HGNC:26921): (poly(ADP-ribose) polymerase family member 6) Enables protein ADP-ribosylase activity. Involved in protein auto-ADP-ribosylation and protein mono-ADP-ribosylation. [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=-0.92).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.994 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001323532.2. 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
	PARP6	NM_001323532.2	MANE Select	c.1192-31A>G		intron	N/A	NP_001310461.1
	PARP6	NM_001323525.2		c.1192-31A>G		intron	N/A	NP_001310454.1
	PARP6	NM_001323528.2		c.1192-31A>G		intron	N/A	NP_001310457.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PARP6	ENST00000569795.6	TSL:5 MANE Select	c.1192-31A>G		intron	N/A	ENSP00000456348.1
	PARP6	ENST00000567974.5	TSL:1	c.988-31A>G		intron	N/A	ENSP00000455815.1
	PARP6	ENST00000419739.7	TSL:1	c.1192-31A>G		intron	N/A	ENSP00000403265.3

Frequencies

GnomAD3 genomes AF: 0.999 AC: 151982 AN: 152170 Hom.: 75898 Cov.: 31

Gnomad AFR AF: 0.996

Gnomad AMI AF: 1.00

Gnomad AMR AF: 1.00

Gnomad ASJ AF: 1.00

Gnomad EAS AF: 1.00

Gnomad SAS AF: 1.00

Gnomad FIN AF: 1.00

Gnomad MID AF: 1.00

Gnomad NFE AF: 1.00

Gnomad OTH AF: 0.999

GnomAD2 exomes AF: 1.00 AC: 246141 AN: 246222 AF XY: 1.00

Gnomad AFR exome AF: 0.996

Gnomad AMR exome AF: 1.00

Gnomad ASJ exome AF: 1.00

Gnomad EAS exome AF: 1.00

Gnomad FIN exome AF: 1.00

Gnomad NFE exome AF: 1.00

Gnomad OTH exome AF: 1.00

GnomAD4 exome AF: 1.00 AC: 1433998 AN: 1434220 Hom.: 716889 Cov.: 24 AF XY: 1.00 AC XY: 715161 AN XY: 715258

African (AFR) AF: 0.996 AC: 32846 AN: 32994

American (AMR) AF: 1.00 AC: 44436 AN: 44446

Ashkenazi Jewish (ASJ) AF: 1.00 AC: 25944 AN: 25944

East Asian (EAS) AF: 1.00 AC: 39496 AN: 39498

South Asian (SAS) AF: 1.00 AC: 85177 AN: 85180

European-Finnish (FIN) AF: 1.00 AC: 53318 AN: 53318

Middle Eastern (MID) AF: 0.999 AC: 5672 AN: 5678

European-Non Finnish (NFE) AF: 1.00 AC: 1087712 AN: 1087752

Other (OTH) AF: 1.00 AC: 59397 AN: 59410

GnomAD4 genome AF: 0.999 AC: 152099 AN: 152288 Hom.: 75956 Cov.: 31 AF XY: 0.999 AC XY: 74371 AN XY: 74460

African (AFR) AF: 0.996 AC: 41369 AN: 41550

American (AMR) AF: 1.00 AC: 15296 AN: 15302

Ashkenazi Jewish (ASJ) AF: 1.00 AC: 3472 AN: 3472

East Asian (EAS) AF: 1.00 AC: 5168 AN: 5168

South Asian (SAS) AF: 1.00 AC: 4820 AN: 4820

European-Finnish (FIN) AF: 1.00 AC: 10618 AN: 10618

Middle Eastern (MID) AF: 1.00 AC: 294 AN: 294

European-Non Finnish (NFE) AF: 1.00 AC: 68038 AN: 68038

Other (OTH) AF: 0.999 AC: 2112 AN: 2114

Alfa AF: 1.00 Hom.: 13779

Bravo AF: 0.999

Asia WGS AF: 1.00 AC: 3478 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.22
DANN	Benign	0.41
PhyloP100		-1.7
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: rs1426166; hg19: chr15-72545876;