rs7662504

Positions:

• chr4-95007419-A-C
• chr4-95007419-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001203.3(BMPR1B):​c.-18+11285A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.445 in 152,014 control chromosomes in the GnomAD database, including 15,544 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 0.44 (15544 hom., cov: 33)
• Consequence: BMPR1B NM_001203.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.454

Genes affected

BMPR1B (HGNC:1077): (bone morphogenetic protein receptor type 1B) This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of 2 different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.705 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
BMPR1B	NM_001203.3	c.-18+11285A>C		intron_variant		ENST00000515059.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
BMPR1B	ENST00000515059.6	c.-18+11285A>C		intron_variant		1	NM_001203.3	P4

Frequencies

GnomAD3 genomes AF: 0.445 AC: 67519 AN: 151896 Hom.: 15524 Cov.: 33

Gnomad AFR AF: 0.481

Gnomad AMI AF: 0.299

Gnomad AMR AF: 0.534

Gnomad ASJ AF: 0.498

Gnomad EAS AF: 0.724

Gnomad SAS AF: 0.279

Gnomad FIN AF: 0.501

Gnomad MID AF: 0.570

Gnomad NFE AF: 0.382

Gnomad OTH AF: 0.469

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

GnomAD4 genome AF: 0.445 AC: 67587 AN: 152014 Hom.: 15544 Cov.: 33 AF XY: 0.448 AC XY: 33322 AN XY: 74316

Gnomad4 AFR AF: 0.481

Gnomad4 AMR AF: 0.533

Gnomad4 ASJ AF: 0.498

Gnomad4 EAS AF: 0.725

Gnomad4 SAS AF: 0.281

Gnomad4 FIN AF: 0.501

Gnomad4 NFE AF: 0.382

Gnomad4 OTH AF: 0.473

Alfa AF: 0.398 Hom.: 18386

Bravo AF: 0.460

Asia WGS AF: 0.501 AC: 1727 AN: 3448

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.0
DANN	Benign	0.76

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

Publications

LitVar

Other links and lift over

dbSNP: rs7662504; hg19: chr4-95928570;