rs6465387

chr7-93524748-C-Gchr7-93524748-C-T

Variant summary

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

The NM_001742.4(CALCR):c.-26-37741G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.237 in 151,904 control chromosomes in the GnomAD database, including 9,216 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 0.24 (9216 hom., cov: 31)
• Consequence: CALCR NM_001742.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0200

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=-0.77).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.621 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CALCR	NM_001742.4	c.-26-37741G>C		intron_variant		ENST00000426151.7
CALCR	NM_001164737.3	c.-97-28774G>C		intron_variant
CALCR	NM_001164738.2	c.-27+34773G>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CALCR	ENST00000426151.7	c.-26-37741G>C		intron_variant		1	NM_001742.4	P1
CALCR	ENST00000394441.5	c.-27+34773G>C		intron_variant		1		P1
CALCR	ENST00000649521.1	c.-97-28774G>C		intron_variant

Frequencies

GnomAD3 genomes AF: 0.237 AC: 35932 AN: 151784 Hom.: 9190 Cov.: 31

Gnomad AFR AF: 0.627

Gnomad AMI AF: 0.0362

Gnomad AMR AF: 0.235

Gnomad ASJ AF: 0.0528

Gnomad EAS AF: 0.355

Gnomad SAS AF: 0.164

Gnomad FIN AF: 0.0720

Gnomad MID AF: 0.139

Gnomad NFE AF: 0.0355

Gnomad OTH AF: 0.204

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

GnomAD4 genome AF: 0.237 AC: 36009 AN: 151904 Hom.: 9216 Cov.: 31 AF XY: 0.239 AC XY: 17714 AN XY: 74256

Gnomad4 AFR AF: 0.627

Gnomad4 AMR AF: 0.236

Gnomad4 ASJ AF: 0.0528

Gnomad4 EAS AF: 0.355

Gnomad4 SAS AF: 0.162

Gnomad4 FIN AF: 0.0720

Gnomad4 NFE AF: 0.0355

Gnomad4 OTH AF: 0.204

Alfa AF: 0.0142 Hom.: 16

Bravo AF: 0.267

Asia WGS AF: 0.296 AC: 1029 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.77
Cadd	Benign	9.4
Dann	Benign	0.83

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: rs6465387; hg19: chr7-93154060;