rs9656015

Positions:

• chr7-93508136-A-G

Variant summary

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

The NM_001742.4(CALCR):​c.-26-21129T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.28 in 152,164 control chromosomes in the GnomAD database, including 6,299 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 0.28 (6299 hom., cov: 32)
• Consequence: CALCR NM_001742.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.447

Genes affected

CALCR (HGNC:1440): (calcitonin receptor) This gene encodes a high affinity receptor for the peptide hormone calcitonin and belongs to a subfamily of seven transmembrane-spanning G protein-coupled receptors. The encoded protein is involved in maintaining calcium homeostasis and in regulating osteoclast-mediated bone resorption. Polymorphisms in this gene have been associated with variations in bone mineral density and onset of osteoporosis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.315 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CALCR	NM_001742.4	c.-26-21129T>C		intron_variant		ENST00000426151.7
CALCR	NM_001164737.3	c.-97-12162T>C		intron_variant
CALCR	NM_001164738.2	c.-26-21129T>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CALCR	ENST00000426151.7	c.-26-21129T>C		intron_variant		1	NM_001742.4	P1
CALCR	ENST00000394441.5	c.-26-21129T>C		intron_variant		1		P1
CALCR	ENST00000649521.1	c.-97-12162T>C		intron_variant

Frequencies

GnomAD3 genomes AF: 0.280 AC: 42580 AN: 152046 Hom.: 6299 Cov.: 32

Gnomad AFR AF: 0.245

Gnomad AMI AF: 0.304

Gnomad AMR AF: 0.219

Gnomad ASJ AF: 0.276

Gnomad EAS AF: 0.113

Gnomad SAS AF: 0.157

Gnomad FIN AF: 0.398

Gnomad MID AF: 0.280

Gnomad NFE AF: 0.318

Gnomad OTH AF: 0.270

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

GnomAD4 genome AF: 0.280 AC: 42598 AN: 152164 Hom.: 6299 Cov.: 32 AF XY: 0.280 AC XY: 20853 AN XY: 74392

Gnomad4 AFR AF: 0.245

Gnomad4 AMR AF: 0.219

Gnomad4 ASJ AF: 0.276

Gnomad4 EAS AF: 0.113

Gnomad4 SAS AF: 0.157

Gnomad4 FIN AF: 0.398

Gnomad4 NFE AF: 0.318

Gnomad4 OTH AF: 0.268

Alfa AF: 0.300 Hom.: 863

Bravo AF: 0.267

Asia WGS AF: 0.137 AC: 477 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	1.1
DANN	Benign	0.44

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: rs9656015; hg19: chr7-93137448;