6-33643890-C-G

Position:

• chr6-33643890-C-G

Variant summary

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

The NM_002224.4(ITPR3):​c.160+3336C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.178 in 152,146 control chromosomes in the GnomAD database, including 3,119 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 0.18 (3119 hom., cov: 32)
• Consequence: ITPR3 NM_002224.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.90

Genes affected

ITPR3 (HGNC:6182): (inositol 1,4,5-trisphosphate receptor type 3) This gene encodes a receptor for inositol 1,4,5-trisphosphate, a second messenger that mediates the release of intracellular calcium. The receptor contains a calcium channel at the C-terminus and the ligand-binding site at the N-terminus. Knockout studies in mice suggest that type 2 and type 3 inositol 1,4,5-trisphosphate receptors play a key role in exocrine secretion underlying energy metabolism and growth. [provided by RefSeq, Aug 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.245 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ITPR3	NM_002224.4	c.160+3336C>G		intron_variant		ENST00000605930.3	NP_002215.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ITPR3	ENST00000605930.3	c.160+3336C>G		intron_variant		1	NM_002224.4	ENSP00000475177.1
ITPR3	ENST00000374316.9	c.160+3336C>G		intron_variant		5		ENSP00000363435.4

Frequencies

GnomAD3 genomes AF: 0.179 AC: 27155 AN: 152028 Hom.: 3121 Cov.: 32

Gnomad AFR AF: 0.0379

Gnomad AMI AF: 0.243

Gnomad AMR AF: 0.228

Gnomad ASJ AF: 0.282

Gnomad EAS AF: 0.147

Gnomad SAS AF: 0.256

Gnomad FIN AF: 0.314

Gnomad MID AF: 0.204

Gnomad NFE AF: 0.224

Gnomad OTH AF: 0.151

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

GnomAD4 genome AF: 0.178 AC: 27153 AN: 152146 Hom.: 3119 Cov.: 32 AF XY: 0.186 AC XY: 13825 AN XY: 74372

Gnomad4 AFR AF: 0.0378

Gnomad4 AMR AF: 0.228

Gnomad4 ASJ AF: 0.282

Gnomad4 EAS AF: 0.148

Gnomad4 SAS AF: 0.257

Gnomad4 FIN AF: 0.314

Gnomad4 NFE AF: 0.224

Gnomad4 OTH AF: 0.149

Alfa AF: 0.132 Hom.: 285

Bravo AF: 0.164

Asia WGS AF: 0.154 AC: 539 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.41
DANN	Benign	0.67

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: rs12205634; hg19: chr6-33611667;