rs2853564

Variant names:

• chr12-47884704-G-A
• rs2853564
• NM_000376.3:c.-83-1930C>T

Variant summary

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

The NM_000376.3(VDR):​c.-83-1930C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.696 in 151,978 control chromosomes in the GnomAD database, including 37,842 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 0.70 (37842 hom., cov: 30)
• Consequence: VDR NM_000376.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.261
• Publications: 58 publications found

Genes affected

VDR (HGNC:12679): (vitamin D receptor) This gene encodes vitamin D3 receptor, which is a member of the nuclear hormone receptor superfamily of ligand-inducible transcription factors. This receptor also functions as a receptor for the secondary bile acid, lithocholic acid. Downstream targets of vitamin D3 receptor are principally involved in mineral metabolism, though this receptor regulates a variety of other metabolic pathways, such as those involved in immune response and cancer. Mutations in this gene are associated with type II vitamin D-resistant rickets. A single nucleotide polymorphism in the initiation codon results in an alternate translation start site three codons downstream. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Jun 2018]

VDR Gene-Disease associations (from GenCC):

• vitamin D-dependent rickets, type 2A

  Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: G2P, Labcorp Genetics (formerly Invitae)
• vitamin D-dependent rickets, type 2

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

ENSG00000205537 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.865 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000376.3. 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
	VDR	NM_000376.3	MANE Select	c.-83-1930C>T		intron	N/A	NP_000367.1	P11473-1
	VDR	NM_001364085.2		c.-83-1930C>T		intron	N/A	NP_001351014.1	A0A5K1VW50
	VDR	NM_001017536.2		c.68-1930C>T		intron	N/A	NP_001017536.1	P11473-2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	VDR	ENST00000549336.6	TSL:1 MANE Select	c.-83-1930C>T		intron	N/A	ENSP00000449573.2	P11473-1
	VDR	ENST00000550325.5	TSL:1	c.68-1930C>T		intron	N/A	ENSP00000447173.1	P11473-2
	VDR	ENST00000395324.6	TSL:5	c.-83-1930C>T		intron	N/A	ENSP00000378734.2	P11473-1

Frequencies

GnomAD3 genomes AF: 0.695 AC: 105595 AN: 151858 Hom.: 37779 Cov.: 30

Gnomad AFR AF: 0.873

Gnomad AMI AF: 0.550

Gnomad AMR AF: 0.729

Gnomad ASJ AF: 0.676

Gnomad EAS AF: 0.660

Gnomad SAS AF: 0.788

Gnomad FIN AF: 0.584

Gnomad MID AF: 0.656

Gnomad NFE AF: 0.597

Gnomad OTH AF: 0.684

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

GnomAD4 genome AF: 0.696 AC: 105717 AN: 151978 Hom.: 37842 Cov.: 30 AF XY: 0.696 AC XY: 51707 AN XY: 74288

African (AFR) AF: 0.873 AC: 36183 AN: 41456

American (AMR) AF: 0.729 AC: 11135 AN: 15266

Ashkenazi Jewish (ASJ) AF: 0.676 AC: 2346 AN: 3470

East Asian (EAS) AF: 0.660 AC: 3399 AN: 5152

South Asian (SAS) AF: 0.787 AC: 3790 AN: 4818

European-Finnish (FIN) AF: 0.584 AC: 6164 AN: 10550

Middle Eastern (MID) AF: 0.651 AC: 190 AN: 292

European-Non Finnish (NFE) AF: 0.597 AC: 40564 AN: 67958

Other (OTH) AF: 0.686 AC: 1444 AN: 2104

Alfa AF: 0.631 Hom.: 134213

Bravo AF: 0.711

Asia WGS AF: 0.732 AC: 2547 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	3.2
DANN	Benign	0.62
PhyloP100		-0.26
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: rs2853564; hg19: chr12-48278487;