NM_006085.6:c.673-263A>G

Variant names:

• chr1-220060054-T-C
• rs34406824
• NM_006085.6:c.673-263A>G

Variant summary

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

The NM_006085.6(BPNT1):​c.673-263A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0498 in 152,256 control chromosomes in the GnomAD database, including 229 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 0.050 (229 hom., cov: 32)
• Consequence: BPNT1 NM_006085.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.481
• Publications: 1 publications found

Genes affected

BPNT1 (HGNC:1096): (3'(2'), 5'-bisphosphate nucleotidase 1) BPNT1, also called bisphosphate 3-prime-nucleotidase, or BPntase, is a member of a magnesium-dependent phosphomonoesterase family. Lithium, a major drug used to treat manic depression, acts as an uncompetitive inhibitor of BPntase. The predicted human protein is 92% identical to mouse BPntase. BPntase's physiologic role in nucleotide metabolism may be regulated by inositol signaling pathways. The inhibition of human BPntase may account for lithium-induced nephrotoxicity. [provided by RefSeq, Jul 2008]

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 (EAS) allele frequency at 95% confidence interval = 0.115 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006085.6. 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
	BPNT1	NM_006085.6	MANE Select	c.673-263A>G		intron	N/A	NP_006076.4
	BPNT1	NM_001286150.2		c.565-263A>G		intron	N/A	NP_001273079.1	O95861-4
	BPNT1	NM_001286149.2		c.508-263A>G		intron	N/A	NP_001273078.1	O95861-3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BPNT1	ENST00000322067.12	TSL:1 MANE Select	c.673-263A>G		intron	N/A	ENSP00000318852.7	O95861-1
	BPNT1	ENST00000916793.1		c.718-263A>G		intron	N/A	ENSP00000586852.1
	BPNT1	ENST00000469520.6	TSL:5	c.673-263A>G		intron	N/A	ENSP00000446828.1	O95861-1

Frequencies

GnomAD3 genomes AF: 0.0496 AC: 7546 AN: 152138 Hom.: 220 Cov.: 32

Gnomad AFR AF: 0.0696

Gnomad AMI AF: 0.00548

Gnomad AMR AF: 0.0415

Gnomad ASJ AF: 0.0660

Gnomad EAS AF: 0.123

Gnomad SAS AF: 0.0425

Gnomad FIN AF: 0.0115

Gnomad MID AF: 0.0696

Gnomad NFE AF: 0.0397

Gnomad OTH AF: 0.0525

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

GnomAD4 genome AF: 0.0498 AC: 7579 AN: 152256 Hom.: 229 Cov.: 32 AF XY: 0.0486 AC XY: 3616 AN XY: 74450

African (AFR) AF: 0.0702 AC: 2915 AN: 41540

American (AMR) AF: 0.0414 AC: 633 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.0660 AC: 229 AN: 3470

East Asian (EAS) AF: 0.123 AC: 638 AN: 5180

South Asian (SAS) AF: 0.0421 AC: 203 AN: 4824

European-Finnish (FIN) AF: 0.0115 AC: 122 AN: 10618

Middle Eastern (MID) AF: 0.0646 AC: 19 AN: 294

European-Non Finnish (NFE) AF: 0.0397 AC: 2699 AN: 68014

Other (OTH) AF: 0.0548 AC: 116 AN: 2116

Alfa AF: 0.0435 Hom.: 52

Bravo AF: 0.0540

Asia WGS AF: 0.0760 AC: 262 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	0.53
PhyloP100		0.48
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: rs34406824; hg19: chr1-220233396;