NM_021127.3:c.59-1186A>G

Variant names:

• chr18-59901461-A-G
• rs7240884
• NM_021127.3:c.59-1186A>G

Variant summary

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

The NM_021127.3(PMAIP1):​c.59-1186A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.552 in 151,988 control chromosomes in the GnomAD database, including 25,529 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 0.55 (25529 hom., cov: 32)
• Consequence: PMAIP1 NM_021127.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.115
• Publications: 7 publications found

Genes affected

PMAIP1 (HGNC:9108): (phorbol-12-myristate-13-acetate-induced protein 1) This gene belongs to a pro-apoptotic subfamily within the BCL-2 protein family, referred to as the BCL-2 homology domain 3 (BH3)-only subfamily, which determine whether a cell commits to apoptosis. In response to death-inducing stimuli, BH3-only members inhibit the anti-apoptotic BCL-2 family members, which under steady-state conditions keep the multi-BH domain proteins BAX and BAK, in an inactive state. [provided by RefSeq, Aug 2020]

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 (AFR) allele frequency at 95% confidence interval = 0.808 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_021127.3. 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
	PMAIP1	NM_021127.3	MANE Select	c.59-1186A>G		intron	N/A	NP_066950.1	A0A0S2Z490
	PMAIP1	NM_001382623.1		c.*879A>G		3_prime_UTR	Exon 2 of 2	NP_001369552.1
	PMAIP1	NM_001382616.1		c.209+883A>G		intron	N/A	NP_001369545.1	Q13794-2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PMAIP1	ENST00000316660.7	TSL:1 MANE Select	c.59-1186A>G		intron	N/A	ENSP00000326119.7	Q13794-1
	PMAIP1	ENST00000269518.9	TSL:1	c.209+883A>G		intron	N/A	ENSP00000269518.9	Q13794-2
	PMAIP1	ENST00000919087.1		c.59-1186A>G		intron	N/A	ENSP00000589146.1

Frequencies

GnomAD3 genomes AF: 0.552 AC: 83763 AN: 151870 Hom.: 25480 Cov.: 32

Gnomad AFR AF: 0.815

Gnomad AMI AF: 0.206

Gnomad AMR AF: 0.506

Gnomad ASJ AF: 0.325

Gnomad EAS AF: 0.717

Gnomad SAS AF: 0.515

Gnomad FIN AF: 0.505

Gnomad MID AF: 0.266

Gnomad NFE AF: 0.418

Gnomad OTH AF: 0.484

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

GnomAD4 genome AF: 0.552 AC: 83866 AN: 151988 Hom.: 25529 Cov.: 32 AF XY: 0.553 AC XY: 41100 AN XY: 74284

African (AFR) AF: 0.815 AC: 33807 AN: 41460

American (AMR) AF: 0.506 AC: 7724 AN: 15264

Ashkenazi Jewish (ASJ) AF: 0.325 AC: 1128 AN: 3468

East Asian (EAS) AF: 0.716 AC: 3705 AN: 5174

South Asian (SAS) AF: 0.513 AC: 2476 AN: 4822

European-Finnish (FIN) AF: 0.505 AC: 5331 AN: 10548

Middle Eastern (MID) AF: 0.259 AC: 76 AN: 294

European-Non Finnish (NFE) AF: 0.418 AC: 28407 AN: 67938

Other (OTH) AF: 0.486 AC: 1024 AN: 2108

Alfa AF: 0.461 Hom.: 30708

Bravo AF: 0.566

Asia WGS AF: 0.587 AC: 2038 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	4.5
DANN	Benign	0.70
PhyloP100		-0.12
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: rs7240884; hg19: chr18-57568693;